Independently manage statistical project support and provide expert consultancy for clinical trial designs and analysis plans. Develop and run SAS programs for data reporting while ensuring compliance with regulatory standards like FDA and ICH.
Worldwide Clinical Trials
129 Remote Job Openings at Worldwide Clinical Trials
Senior Director of Clinical Projects, Clinical Assessment Technologies
Worldwide Clinical Trials
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Full Time
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3 days ago
Worldwide Clinical Trials
Accountable for the oversight of clinical activities and protocols for Clinical Assessment Technologies, including training development and data surveillance. Leads departmental strategic initiatives, manages clinical staff, and ensures compliance with SOPs and regulatory guidelines.
Medical Director, Medical Affairs - US - Remote
Worldwide Clinical Trials
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Full Time
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3 days ago
Worldwide Clinical Trials
The Medical Director provides medical management and professional support for clinical research projects as a Medical Monitor. Responsibilities include managing clinical trials, processing Serious Adverse Events, and contributing medical input to study protocols and development programs.
Senior Manager, Clinical Operations Site Management (Franchise Lead) - Europe - Remote
Worldwide Clinical Trials
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Full Time
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3 days ago
Worldwide Clinical Trials
Provide therapeutic and operational expertise to ensure projects within the franchise are properly resourced and delivered effectively. Coordinate between project management, site management, and study start-up while managing quality metrics and direct reports.
Project Manager - Oncology - US/Canada - Remote
Worldwide Clinical Trials
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Full Time
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3 days ago
Worldwide Clinical Trials
The Project Manager is responsible for the overall coordination and management of clinical trials from start-up through closeout. This includes directing technical, financial, and operational aspects to ensure deliverables meet customer time, quality, and cost expectations.
Senior Clinical Trials Associate
Worldwide Clinical Trials
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Full Time
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3 days ago
Worldwide Clinical Trials
The Senior Clinical Trials Associate provides administrative and project tracking support to the clinical project team. Key duties include maintaining project portals, managing trial master files, and coordinating training for the project team.
Senior Clinical Research Associate - Rare CNS - Southeast/Mid-Atlantic (Remote)
Worldwide Clinical Trials
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Full Time
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4 days ago
Worldwide Clinical Trials
Manage research activities at clinical sites, including site identification, start-up, and close-out. Ensure compliance with regulatory requirements and safety reporting while conducting study initiation visits.
Senior Clinical Research Associate - Oncology/Rare Disease - Texas (Remote)
Worldwide Clinical Trials
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Full Time
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4 days ago
Worldwide Clinical Trials
Manage research activities at clinical sites, including site identification, start-up, and close-down. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
Senior Clinical Research Associate - Rare CNS - Southeast/Mid-Atlantic (Remote)
Worldwide Clinical Trials
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Full Time
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4 days ago
Worldwide Clinical Trials
Manage research activities at clinical sites, including site identification, start-up, and close-out activities. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
Senior Clinical Research Associate - CNS/Rare Disease - Central U.S. (Remote)
Worldwide Clinical Trials
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Full Time
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4 days ago
Worldwide Clinical Trials
Manage research activities at clinical sites, including site identification, start-up activities, and study maintenance. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
Senior Clinical Trial Manager - Oncology - U.S. (Remote)
Worldwide Clinical Trials
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Full Time
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4 days ago
Worldwide Clinical Trials
Provide leadership and direction to clinical site management teams from study start through closure. Serve as the primary point of contact for sponsors regarding clinical monitoring and site activities while managing deliverables and budgets.
Project Manager - Oncology - Australia - Remote
Worldwide Clinical Trials
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Full Time
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4 days ago
Worldwide Clinical Trials
The Project Manager is responsible for the overall coordination and management of clinical trials from start-up through closeout. This includes directing technical, financial, and operational aspects to ensure deliverables meet customer expectations for time, quality, and cost.
Clinical Research Associate - Neurology, Oncology - Germany
Worldwide Clinical Trials
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Full Time
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5 days ago
Worldwide Clinical Trials
The CRA is responsible for managing the full lifecycle of clinical sites, including qualification, initiation, monitoring, and close-out visits. They ensure protocol adherence, verify source documents for data veracity, and manage site documentation within the Trial Master File.
Clinical Research Associate - Oncology, Hematology - Italy
Worldwide Clinical Trials
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Full Time
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5 days ago
Worldwide Clinical Trials
The CRA is responsible for the full lifecycle of site management, including qualification, initiation, monitoring, and close-out visits. Key duties include verifying source documents, ensuring protocol adherence, and managing Trial Master File documentation.
Lead strategic business transformation projects and design financial organizational structures to enhance profitability and efficiency. Collaborate with executive management and the board to translate corporate strategies into actionable financial plans and forecasts.
Senior Clinical Research Associate (Bilingual) - Oncology - Canada (Remote)
Worldwide Clinical Trials
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Full Time
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5 days ago
Worldwide Clinical Trials
Manage research activities at clinical sites, including site identification, start-up activities, and study maintenance. Conduct site initiation visits and ensure compliance with regulatory requirements and safety reporting.
Senior Clinical Research Associate - Oncology - Brazil - Remote
Worldwide Clinical Trials
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Full Time
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5 days ago
Worldwide Clinical Trials
Responsible for the full lifecycle of site management, including qualification, initiation, monitoring, and close-out visits. The role involves ensuring protocol adherence, verifying source documents, and mentoring less experienced CRAs.
Senior Associate II, TMF Operations - EMEA/LATAM- Fixed term- Remote
Worldwide Clinical Trials
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Full Time
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5 days ago
Worldwide Clinical Trials
Manage complex studies or sponsor portfolios by performing RMC Lead activities and providing subject matter expertise on TMF needs. Oversee quality control processes, develop TMF quality management documents, and present KPI trends to project teams and sponsors.
Executive Director, Therapeutic Strategy Lead, Oncology
Worldwide Clinical Trials
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Full Time
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6 days ago
Worldwide Clinical Trials
The Oncology Therapeutic Strategy Lead serves as a therapeutic consultant, supporting the Business Development organization and Therapeutic Area Leads. This role involves creating effective delivery strategies for clinical trials and collaborating with various internal teams to achieve new business targets.
Site Activation Manager
Worldwide Clinical Trials
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Full Time
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6 days ago
Worldwide Clinical Trials
Accountable for site activation project management and delivery within the Oncology therapeutic area, including oversight of site identification and regulatory activities. Responsible for tracking metrics, managing budgets, and communicating status and risks to sponsors and internal leadership.
Site Activation Manager
Worldwide Clinical Trials
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Full Time
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6 days ago
Worldwide Clinical Trials
The Site Activation Manager is responsible for project management and delivery of site activation activities within the Oncology therapeutic area. This includes overseeing site identification, regulatory document collection, and ensuring compliance with GCP and SOPs.
Contract Manager - US - Remote
Worldwide Clinical Trials
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Full Time
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6 days ago
Worldwide Clinical Trials
Manage the full lifecycle of sponsor contracts and change orders, including drafting, budgeting, and negotiating terms. Collaborate with cross-functional departments to ensure legal, financial, and operational compliance.
PRN Data Coordinator - US - Remote
Worldwide Clinical Trials
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Full Time
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6 days ago
Worldwide Clinical Trials
The Data Coordinator ensures source data from clinical trials is accurately transcribed into Case Report Forms according to Good Clinical Practice guidelines. They are also responsible for reviewing study protocols and reconciling study records for archiving.
Marketing Summer Intern
Worldwide Clinical Trials
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Full Time
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7 days ago
Worldwide Clinical Trials
The intern will support the Global Marketing team with a focus on demand operations, marketing data integrity, and process optimization. Key tasks include campaign setup, performance reporting, and maintaining the department's SharePoint and digital marketing efforts.
Clinical Trials Associate - Europe
Worldwide Clinical Trials
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Full Time
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10 days ago
Worldwide Clinical Trials
Provide administrative and project tracking support to the clinical project team to ensure tasks are performed accurately and timely. Responsibilities include managing system access, auditing project portals, and maintaining the trial master file.
Senior Director, Business Development - French Speaking - UK/Europe - Remote
Worldwide Clinical Trials
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Full Time
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11 days ago
Worldwide Clinical Trials
Drive revenue growth by identifying new business opportunities and securing contracts for Phase I-IV clinical studies. Manage key accounts and coordinate responses to Requests for Proposals and Information while representing the company at trade shows.
Senior Project Manager - Oncology - US/Canada - Remote
Worldwide Clinical Trials
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Full Time
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11 days ago
Worldwide Clinical Trials
The Senior Project Manager coordinates clinical trials from start-up through closeout, managing technical, financial, and operational aspects. They collaborate with functional leads to ensure all project deliverables meet customer time, quality, and cost expectations.
Senior Clinical Research Associate - Oncology - Central U.S. (Remote)
Worldwide Clinical Trials
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Full Time
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13 days ago
Worldwide Clinical Trials
Manage research activities at clinical sites, including site identification, start-up, and close-out. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
Patient and Site Solutions- Project Manager - UK - Remote
Worldwide Clinical Trials
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Full Time
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13 days ago
Worldwide Clinical Trials
Lead the end-to-end delivery of patient and site engagement activities across multiple clinical studies. Coordinate global vendors and manage project plans, budgets, and timelines to ensure recruitment objectives are met.
Senior Clinical Research Associate - Rare Disease - East Coast/Central (Remote)
Worldwide Clinical Trials
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Full Time
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13 days ago
Worldwide Clinical Trials
Manage research activities at clinical sites, including site identification, start-up, and close-down processes. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
Senior Clinical Research Associate, CNS - West Coast - Remote
Worldwide Clinical Trials
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Full Time
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14 days ago
Worldwide Clinical Trials
Manage research activities at clinical sites, including site identification, start-up, and close-out activities. Ensure compliance with regulatory requirements, informed consent, and safety reporting through remote and on-site monitoring.
Senior / Project Manager - Cardiometabolic/Early Phase - Australia - Remote
Worldwide Clinical Trials
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Full Time
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14 days ago
Worldwide Clinical Trials
The Project Manager is responsible for the overall coordination and management of clinical trials from start-up through closeout. This includes directing technical, financial, and operational aspects to ensure deliverables meet customer time, quality, and cost expectations.
Senior/Specialist, Regulatory Affairs - Serbia- Remote
Worldwide Clinical Trials
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Full Time
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14 days ago
Worldwide Clinical Trials
Manage and track regulatory submissions for clinical trials in Serbia, ensuring compliance with local and international regulations. Liaise with project teams to provide strategic guidance on documentation, labeling, and regulatory intelligence.
Senior Clinical Research Associate - CNS/Early Phase - Australia - Remote
Worldwide Clinical Trials
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Full Time
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14 days ago
Worldwide Clinical Trials
Responsible for the full lifecycle of site management, including qualification, initiation, monitoring, and close-out visits. The role involves ensuring protocol adherence, verifying source documents, and mentoring less experienced CRAs.
Assistant, Regulatory Affairs Europe- Remote
Worldwide Clinical Trials
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Full Time
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14 days ago
Worldwide Clinical Trials
The role involves coordinating the translation and dispatch of regulatory submissions, site contracts, and labels. It also includes performing administrative quality control and managing therapeutic mailboxes to triage requests.
Principal Market Analysis and Corporate Strategy
Worldwide Clinical Trials
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Full Time
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17 days ago
Worldwide Clinical Trials
Lead business analytics for the commercial organization by tracking KPIs, pipeline, and win rates to drive strategic decisions. Conduct continual market trend assessments and partner with leadership to develop global sales targets and pricing strategies.
Senior Director, Business Development - US
Worldwide Clinical Trials
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Full Time
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17 days ago
Worldwide Clinical Trials
Drive revenue growth by proactively marketing CRO services and identifying new leads for clinical, bioanalytical, and ADME business. Manage the full sales cycle, including writing proposals, delivering client presentations, and maintaining CRM data.
Associate Director / Director, Project Management - Renal diseases - US/Canada - Remote
Worldwide Clinical Trials
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Full Time
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17 days ago
Worldwide Clinical Trials
Accountable for directing multiple clinical projects simultaneously to ensure delivery within cost, time, and quality requirements. Acts as a liaison for business development and collaborates across functional areas to improve business processes.
Senior / Project Manager - Oncology - Europe - Remote
Worldwide Clinical Trials
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Full Time
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17 days ago
Worldwide Clinical Trials
The Senior Project Manager is responsible for the overall coordination and management of clinical trials from start-up through closeout. This includes directing technical, financial, and operational aspects to ensure deliverables meet customer expectations for time, quality, and cost.
Specialist, Site Contracts - REMOTE - Argentina or Brazil
Worldwide Clinical Trials
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Full Time
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18 days ago
Worldwide Clinical Trials
Responsible for the development, negotiation, and finalization of Site Agreements and amendments for clinical research sites. This includes managing budgets, liaising with legal and data privacy teams, and maintaining tracking tools for contract lifecycles.
Associate Director, Operations - Clinical Assessment Technologies (CAT) - US/Canada - Remote
Worldwide Clinical Trials
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Full Time
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18 days ago
Worldwide Clinical Trials
The role involves providing operational oversight and resource management for Clinical Assessment Technologies (CAT) study projects. Key duties include managing study deliverables, coordinating with vendors, and contributing to business development activities and process improvements.
Associate Director, Operations - Clinical Assessment Technologies CAT) - UK/Europe - Remote
Worldwide Clinical Trials
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Full Time
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18 days ago
Worldwide Clinical Trials
Oversee operational activities for Clinical Assessment Technologies (CAT) projects, including resource management and vendor oversight. Lead departmental initiatives, manage study deliverables from launch to close-out, and support business development activities.
Site Contracts Specialist - Europe - Remote
Worldwide Clinical Trials
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Full Time
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18 days ago
Worldwide Clinical Trials
The role involves drafting, negotiating, and finalizing clinical research site agreements and budgets. It also requires coordinating with legal, data privacy, and study teams to ensure contract execution and tracking.
Clinical Research Associate - Germany - Oncology, Hematology, CNS, Cardiometabolic
Worldwide Clinical Trials
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Full Time
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18 days ago
Worldwide Clinical Trials
The CRA is responsible for the full lifecycle of site management, including qualification, initiation, monitoring, and close-out visits. They ensure protocol adherence, verify source documents for data veracity, and manage Trial Master File documentation.
Specialist, Site Contracts
Worldwide Clinical Trials
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Full Time
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19 days ago
Worldwide Clinical Trials
The Specialist is responsible for developing, negotiating, and finalizing Site Agreements and amendments between sponsors and clinical research sites. This includes managing budgets, ensuring regulatory compliance, and coordinating with legal and study teams to facilitate contract execution.
Manager, Clinical Operations Site Management (Franchise Lead) - CNS - U.S. (Remote)
Worldwide Clinical Trials
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Full Time
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19 days ago
Worldwide Clinical Trials
Responsible for the on-time and quality delivery of site management services within the CNS therapeutic area. This includes managing CRA performance, coordinating with project management, and ensuring proper resourcing and training for franchise projects.
Vendor Contracts Manager (Contract-to-Hire) - U.S. - Remote
Worldwide Clinical Trials
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Full Time
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19 days ago
Worldwide Clinical Trials
Responsible for preparing, reviewing, and managing the execution of vendor contracts by incorporating budgets and scopes of work. The role involves tracking documentation, handling secondary negotiations, and maintaining internal and external stakeholder relationships.
Associate Director, Contract Management - US - Remote
Worldwide Clinical Trials
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Full Time
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19 days ago
Worldwide Clinical Trials
The Associate Director manages all aspects of contract management, including MSAs and change orders, for sponsors. They provide legal contractual strategy and collaborate with BD, Finance, and Operations to ensure agreements reflect operational needs.
eQMS System Administrator - Europe - Remote
Worldwide Clinical Trials
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Full Time
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19 days ago
Worldwide Clinical Trials
Responsible for the secure and compliant administration of user access and roles within the eQMS Quality Management System. Provides subject matter expertise for system support, audit readiness, and the migration of documents to eQMS Binders.
Strategic Sourcing Analyst - US - Remote
Worldwide Clinical Trials
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Full Time
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19 days ago
Worldwide Clinical Trials
Responsible for securing third-party vendors and implementing sourcing and category management strategies to support global clinical trials. The role involves managing assigned commodities and maintaining high-quality vendor relationships to meet corporate business objectives.
Senior Clinical Research Associate - CNS/Psychiatry - Midwest (Remote)
Worldwide Clinical Trials
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Full Time
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19 days ago
Worldwide Clinical Trials
Manage research activities at clinical sites, including site identification, start-up, and close-out. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
Senior Clinical Trial Manager - CNS - U.S. (Remote)
Worldwide Clinical Trials
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Full Time
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20 days ago
Worldwide Clinical Trials
Provide leadership and direction to clinical site management teams from study start through closure. Serve as the primary point of contact for sponsors regarding clinical monitoring and site activities.
Senior / Project Quality Assurance Lead - US/Canada - Remote
Worldwide Clinical Trials
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Full Time
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20 days ago
Worldwide Clinical Trials
The role involves acting as a GCP Subject Matter Expert to ensure study protocol compliance and managing root cause analysis for quality issues. The lead will also perform quality reviews, support site inspections, and manage the QA relationship with sponsors.
Senior Project Manager - Cardiometabolic - US/Canada - Remote
Worldwide Clinical Trials
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Full Time
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20 days ago
Worldwide Clinical Trials
The Senior Project Manager coordinates and manages clinical trials from start-up through closeout, directing technical, financial, and operational aspects. They collaborate with functional leads to ensure all project deliverables meet customer expectations regarding time, quality, and cost.
Senior Clinical Research Associate - CNS/Psychiatry - West Coast - Remote
Worldwide Clinical Trials
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Full Time
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21 days ago
Worldwide Clinical Trials
Manage research activities at clinical sites, including site identification, start-up, and close-down. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
Clinical Research Associate II - Psychiatry - United States (Remote)
Worldwide Clinical Trials
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Full Time
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21 days ago
Worldwide Clinical Trials
Manage research activities at clinical sites, including site identification, start-up activities, and regulatory document collection. Conduct study initiation visits and ensure compliance with informed consent and safety reporting throughout the study lifecycle.
Clinical Research Associate II - Oncology - United States (Remote)
Worldwide Clinical Trials
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Full Time
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21 days ago
Worldwide Clinical Trials
Manage research activities at clinical sites, including site identification, start-up, and close-down. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
Senior Recruiter - UK - Remote
Worldwide Clinical Trials
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Full Time
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25 days ago
Worldwide Clinical Trials
The Senior Recruiter manages the full recruitment lifecycle and partners with hiring managers to develop effective talent acquisition strategies. They are responsible for sourcing qualified candidates, maintaining talent pipelines, and ensuring a high-quality candidate experience.
Clinical Supply Specialist - Argentina/Europe- Remote
Worldwide Clinical Trials
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Full Time
·
a month ago
Worldwide Clinical Trials
The specialist will plan, implement, and monitor the overall study supply chain strategy to maximize efficiency and minimize costs. This includes managing inventories of study drugs and collaborating with project management and vendors to optimize delivery processes.
Manager, Data Management - Serbia - Remote
Worldwide Clinical Trials
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Full Time
·
a month ago
Worldwide Clinical Trials
Provide leadership and oversight for Data Management teams and projects, focusing on study execution and budget management. Act as the primary point of contact for escalations and represent the company at sponsor governance meetings.
Clinical Payments Associate - Europe/LATAM - Remote
Worldwide Clinical Trials
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Full Time
·
a month ago
Worldwide Clinical Trials
The role involves managing administrative tasks, triaging tickets and emails in Jira, and responding to payment queries from sites and sponsors. Additionally, the associate supports system migrations and study reconciliation activities through data preparation and tracking.
Specialist, Proposals & Client Services - US - Remote
Worldwide Clinical Trials
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Full Time
·
a month ago
Worldwide Clinical Trials
The Specialist manages the end-to-end proposal process, including the preparation of RFPs, RFIs, and complex budget tools. They collaborate with account directors and operational teams to refine scopes and ensure comprehensive client service delivery.
Specialist, Site Contracts - Australia - Remote
Worldwide Clinical Trials
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Full Time
·
a month ago
Worldwide Clinical Trials
The role involves drafting, negotiating, and finalizing clinical research site agreements and budgets. It also requires coordinating with legal, regulatory, and study teams to ensure contract execution and tracking.
Team Lead, TMF Operations - Europe - Remote
Worldwide Clinical Trials
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Full Time
·
a month ago
Worldwide Clinical Trials
The Team Lead is responsible for maintaining Trial Master Files inspection readiness in compliance with SOPs, ALCOA principles, and industry regulations. They drive project team objectives and oversee TMF services for multiple studies while managing risks and KPIs.
Inside Sales Development Account Manager
Worldwide Clinical Trials
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Full Time
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a month ago
Worldwide Clinical Trials
The role focuses on sourcing new sales opportunities through inbound lead qualification and outbound prospecting to drive revenue growth. The manager will engage prospects, set appointments for Business Development partners, and manage sales territories using Salesforce.
Backlog & Revenue Lead - U.S. - Remote
Worldwide Clinical Trials
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Full Time
·
a month ago
Worldwide Clinical Trials
The Backlog & Revenue Lead manages the end-to-end governance of order backlog and revenue realization to ensure predictable conversion. This includes orchestrating cross-functional processes between Sales, Finance, and Operations while providing decision-ready insights and forecast accuracy.
Senior Proposal Associate - RFIs - Mexico/US - Remote
Worldwide Clinical Trials
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Full Time
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a month ago
Worldwide Clinical Trials
Lead the development, writing, and coordination of robust responses to RFIs using Microsoft Word and Excel. Collaborate with Subject Matter Experts and Account Directors to ensure accurate product offerings and maintain the content library.
Senior Clinical Research Associate - CNS/Rare Disease - Midwest - Remote
Worldwide Clinical Trials
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Full Time
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a month ago
Worldwide Clinical Trials
Manage research activities at clinical sites, including site identification, start-up, and close-out. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
Associate Director, FP&A - US - Remote
Worldwide Clinical Trials
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Full Time
·
a month ago
Worldwide Clinical Trials
The Associate Director of FP&A supports complex financial planning, reporting, and analysis to drive data-driven decision making. Key duties include producing monthly board reports, managing forecasts and budgets, and partnering with corporate functions to achieve financial targets.
Senior Clinical Research Associate - Oncology - Central - Remote
Worldwide Clinical Trials
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Full Time
·
a month ago
Worldwide Clinical Trials
Manage research activities at clinical sites, including site identification, start-up, and close-out activities. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
Specialist, Regulatory Affairs - Poland - Remote
Worldwide Clinical Trials
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Full Time
·
a month ago
Worldwide Clinical Trials
Manage and track regulatory submissions for clinical trials in Poland, ensuring compliance with EU-CTR and local regulations. Liaise with project teams to provide strategic guidance on documentation, labeling, and patient consent forms.
Regulatory Affairs Specialist - Czechia - Remote
Worldwide Clinical Trials
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Full Time
·
a month ago
Worldwide Clinical Trials
The role involves managing and submitting regulatory dossiers and coordinating with ethics committees to ensure clinical trial compliance. It also requires maintaining country-specific intelligence and advising project teams on regulatory strategies and legislation.
Specialist, Regulatory & Site Activation - Brazil - Remote
Worldwide Clinical Trials
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Full Time
·
a month ago
Worldwide Clinical Trials
Liaise with colleagues to organize and submit high-quality regulatory documentation on a timely basis. Maintain country-specific patient information, consent forms, and drug labeling to ensure compliance with ICH GCP and local requirements.
Senior Clinical Research Associate - CNS/Oncology - West Coast
Worldwide Clinical Trials
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Full Time
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a month ago
Worldwide Clinical Trials
Manage research activities at clinical sites, including site identification, start-up, and close-out. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
Senior Clinical Research Associate - CNS/Psychiatry/Rare Disease - West Coast - Remote
Worldwide Clinical Trials
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Full Time
·
a month ago
Worldwide Clinical Trials
Manage research activities at clinical sites, including site identification, start-up, and close-out. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
Senior Clinical Research Associate - CNS/Oncology - West Coast
Worldwide Clinical Trials
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Full Time
·
a month ago
Worldwide Clinical Trials
Manage research activities at clinical sites, including site identification, start-up, and close-out. Conduct study initiation visits and ensure compliance with informed consent and safety reporting requirements.
Senior Clinical Research Associate - CNS/Rare Disease - Midwest - Remote
Worldwide Clinical Trials
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Full Time
·
a month ago
Worldwide Clinical Trials
Manage research activities at clinical sites, including site identification, start-up, and close-down. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
Senior Clinical Research Associate - CNS/Psychiatry - Northeast - Remote
Worldwide Clinical Trials
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Full Time
·
a month ago
Worldwide Clinical Trials
Manage research activities at clinical sites, including site identification, start-up, and close-out activities. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
Senior Clinical Research Associate - CNS/Oncology - Midwest - Remote
Worldwide Clinical Trials
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Full Time
·
a month ago
Worldwide Clinical Trials
Manage research activities at clinical sites, including identification, start-up, maintenance, and close-out phases. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
Oversee and lead data management services across multiple complex global clinical projects from startup to closeout. Ensure accurate trial documentation, effective UAT, and timely database locks while managing resources and budgets.
Senior Clinical Research Associate - Oncology, Hematology - France
Worldwide Clinical Trials
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Full Time
·
a month ago
Worldwide Clinical Trials
The role is responsible for the full lifecycle of site management, including qualification, initiation, monitoring, and close-out visits. It also involves mentoring junior CRAs and ensuring strict protocol adherence and data veracity through source document verification.
Director, Regulatory Pre-Award Strategy - UK- Remote
Worldwide Clinical Trials
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Full Time
·
a month ago
Worldwide Clinical Trials
Lead the operational strategy and growth objectives for global regulatory affairs, overseeing the delivery of regulatory activities and supporting roles. Drive business development efforts by contributing to proposals, bid defense meetings, and regulatory costing for site activation strategies.
The Project Manager is responsible for the overall coordination and management of clinical trials from start-up through closeout. This includes directing technical, financial, and operational aspects to ensure deliverables meet customer expectations for time, quality, and cost.
Senior Compensation Contractor - Remote - US
Worldwide Clinical Trials
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Full Time
·
a month ago
Worldwide Clinical Trials
Provide project-based support for global compensation, focusing on M&A integration and salary/bonus harmonization. Perform market pricing and benchmarking to build compensation models and support organizational changes.
Commercial IT Business Partner
Worldwide Clinical Trials
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Full Time
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a month ago
Worldwide Clinical Trials
Acts as the strategic technology liaison between IT and the Commercial organization to align technology investments with business growth. Leads the optimization of commercial systems, specifically Salesforce, across the lead-to-cash lifecycle.
Project Manager - South Korea - Remote
Worldwide Clinical Trials
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Full Time
·
a month ago
Worldwide Clinical Trials
The Project Manager is responsible for the overall coordination and management of clinical trials from start-up through closeout. This includes directing technical, financial, and operational aspects to ensure deliverables meet customer expectations for time, quality, and cost.
Global Vice President, Therapeutic Strategy
Worldwide Clinical Trials
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Full Time
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a month ago
Worldwide Clinical Trials
Provide strategic leadership and therapeutic expertise across Oncology, Rare Disease, Cardio Metabolic, and Neuroscience to drive business growth. Partner with commercial and operational teams to develop innovative clinical strategies and lead a team of Therapeutic Strategy Leads.
Conference and Events Coordinator - US - Remote
Worldwide Clinical Trials
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Full Time
·
a month ago
Worldwide Clinical Trials
The coordinator supports the planning and execution of global conferences and events to align with marketing and business objectives. Key tasks include managing logistics, coordinating with vendors, and collaborating with cross-functional teams to ensure seamless event delivery.
Senior Director, Data Intelligence
Worldwide Clinical Trials
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Full Time
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a month ago
Worldwide Clinical Trials
The Senior Director will shape and own the enterprise data intelligence strategy, translating complex analytics into executive narratives to influence company direction. They will serve as a primary advisor to the Senior Leadership Team and oversee the delivery of internal and external reporting portfolios.
Senior Clinical Research Associate - CNS/Psychiatry - West Coast - Remote
Worldwide Clinical Trials
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Full Time
·
a month ago
Worldwide Clinical Trials
Manage research activities at clinical sites, including site identification, start-up, and close-down. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
Principal Identity Governance and Administration - US - Remote
Worldwide Clinical Trials
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Full Time
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2 months ago
Worldwide Clinical Trials
Lead the architecture, engineering, and operational delivery of enterprise Identity and Access Management (IAM) capabilities. Design and implement scalable identity solutions and automate lifecycle processes across a global, regulated environment.
Senior Manager, Regulatory Affairs - Europe - remote
Worldwide Clinical Trials
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Full Time
·
2 months ago
Worldwide Clinical Trials
Manage regulatory and ethics committee submissions across EMEA, Asia Pacific, and Latin America while ensuring compliance with global standards. Provide strategic regulatory advice, support business development activities, and mentor junior staff members.
Workday Adaptive Planning Architect - US - Remote
Worldwide Clinical Trials
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Full Time
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2 months ago
Worldwide Clinical Trials
The Architect serves as the enterprise owner and strategic leader for the Workday Adaptive Planning platform, overseeing the product vision and roadmap. They partner with Finance and HR leadership to design secure, high-performing models and integrations aligned with business strategy.
Risk Strategy Director - Fixed Term - UK - Remote
Worldwide Clinical Trials
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Full Time
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2 months ago
Worldwide Clinical Trials
The Director of Risk Strategy provides functional leadership and subject matter expertise in Risk-Based Quality Management (RBQM) for both internal teams and sponsors. They lead the design of cross-functional RBQM strategies, manage departmental processes, and ensure compliance with GCP and regulatory guidelines.
Senior Project Quality Assurance Lead - Europe - Remote
Worldwide Clinical Trials
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Full Time
·
2 months ago
Worldwide Clinical Trials
Lead quality assurance activities and deliverables across complex global studies, acting as a GCP subject matter expert. Manage investigations, root cause analysis, and CAPA plans while collaborating with project teams and sponsors to ensure regulatory compliance.
Senior Clinical Research Associate - Oncology - East Coast - Remote
Worldwide Clinical Trials
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Full Time
·
2 months ago
Worldwide Clinical Trials
Responsible for managing all stages of clinical research activities at study sites, including qualification, initiation, monitoring, and close-out. Ensures data quality and compliance with GCP, local regulations, and SOPs while managing safety event reporting.
Team Lead, TMF Operations - Argentina- Remote
Worldwide Clinical Trials
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Full Time
·
2 months ago
Worldwide Clinical Trials
The Team Lead ensures Trial Master Files inspection readiness in compliance with SOPs, ALCOA principles, and industry regulations. They oversee TMF services for multiple studies and manage the delivery of project team objectives regarding essential documents.
Clinical Trials Associate
Worldwide Clinical Trials
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Full Time
·
2 months ago
Worldwide Clinical Trials
The Clinical Trials Associate provides administrative and project tracking support to the clinical project team. Key duties include maintaining project portals, managing trial master files, and coordinating project-specific training.
Senior Clinical Research Associate-Oncology-Brazil (Remote)
Worldwide Clinical Trials
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Full Time
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2 months ago
Worldwide Clinical Trials
Manage research activities at clinical sites, including site identification, start-up, and close-down. Ensure compliance with regulatory requirements, informed consent, and safety reporting through remote and on-site monitoring.
Senior Project Manager - US - Remote
Worldwide Clinical Trials
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Full Time
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2 months ago
Worldwide Clinical Trials
The Senior Project Manager coordinates clinical trials from start-up to closeout, managing technical, financial, and operational aspects. They collaborate with functional leads to ensure project deliverables meet customer expectations regarding time, quality, and cost.
Specialist, Regulatory & Site Activation - South Korea- Remote
Worldwide Clinical Trials
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Full Time
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2 months ago
Worldwide Clinical Trials
Liaise with colleagues to organize and submit high-quality regulatory submissions on a timely basis. Maintain country-specific patient information, consent forms, and drug labeling to ensure compliance with ICH GCP and local requirements.
Senior Clinical Research Associate - Psychiatry - East Coast - Remote
Worldwide Clinical Trials
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Full Time
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2 months ago
Worldwide Clinical Trials
Manage research activities at clinical sites, including site identification, start-up, and close-down processes. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
Senior Project Manager - CNS - US/Canada - Remote
Worldwide Clinical Trials
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Full Time
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2 months ago
Worldwide Clinical Trials
The Senior Project Manager is responsible for the overall coordination and management of clinical trials from start-up through closeout. This includes directing technical, financial, and operational aspects to ensure deliverables meet customer time, quality, and cost expectations.
Senior Clinical Research Associate, Oncology - Argentina - Remote
Worldwide Clinical Trials
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Full Time
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2 months ago
Worldwide Clinical Trials
Manage research activities at clinical sites, including site identification, start-up, and close-down. Ensure compliance with regulatory requirements, informed consent, and safety reporting during study maintenance.
Contractor Senior Clinical Research Associate - Contractor - UK
Worldwide Clinical Trials
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Full Time
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2 months ago
Worldwide Clinical Trials
The Senior Clinical Research Associate is responsible for site qualification, monitoring, and management to ensure protocol adherence and data integrity. They also provide mentorship to less experienced staff and ensure all site documentation is accurately filed in the Trial Master File.
Clinical Scientist - Oncology - US - Remote
Worldwide Clinical Trials
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Full Time
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3 months ago
Worldwide Clinical Trials
The Clinical Scientist leads the assessment of clinical data to ensure quality and integrity while translating complex findings into actionable insights for internal teams and clients. They collaborate with cross-functional stakeholders to support regulatory deliverables, monitor safety events, and drive study execution strategies.
Risk and Central Monitoring Manager - Argentina/Mexico - Remote
Worldwide Clinical Trials
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Full Time
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3 months ago
Worldwide Clinical Trials
The Risk and Central Monitoring Manager coordinates cross-functional risk management and central monitoring activities for clinical trials in accordance with ICH GCP guidelines. They are responsible for developing monitoring strategies, overseeing risk-based quality management activities, and ensuring inspection readiness throughout the study lifecycle.
Senior Director, Business Development - West Coast - Remote
Worldwide Clinical Trials
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Full Time
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3 months ago
Worldwide Clinical Trials
The Senior Director of Business Development is responsible for driving revenue growth by identifying new business opportunities and managing client relationships within the clinical research industry. They lead proposal development, conduct bid defense meetings, and coordinate strategic interactions between sponsors and internal project teams.
Director, Business Development - West Coast - Remote
Worldwide Clinical Trials
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Full Time
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3 months ago
Worldwide Clinical Trials
The Director of Business Development is responsible for achieving revenue objectives by identifying new business leads and managing client relationships within the clinical research industry. They will lead proposal development, conduct bid defense meetings, and coordinate strategic efforts with internal teams to secure new contracts.
Senior Proposal Manager - Writing - LATAM - Remote
Worldwide Clinical Trials
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Full Time
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3 months ago
Worldwide Clinical Trials
The Senior Proposal Manager leads the writing, coordination, and presentation of complex proposals while collaborating with subject matter experts and account directors. They also mentor junior writers and drive process improvement initiatives to ensure high-quality, timely deliverables.
Site Activation Manager - Europe/US - Remote
Worldwide Clinical Trials
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Full Time
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3 months ago
Worldwide Clinical Trials
The Site Activation Manager is responsible for overseeing site activation project management and delivery activities within the CNS therapeutic area. They ensure milestones are met on time and within budget while coordinating cross-functional activities and maintaining regulatory compliance.
Project Manager - US - Remote
Worldwide Clinical Trials
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Full Time
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3 months ago
Worldwide Clinical Trials
The Project Manager is responsible for the end-to-end coordination and management of clinical trials from start-up through closeout. They direct the technical, financial, and operational aspects of projects to ensure deliverables meet time, quality, and cost expectations.
Associate II, TMF Operations - UK - Remote
Worldwide Clinical Trials
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Full Time
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3 months ago
Worldwide Clinical Trials
The role involves performing TMF quality control reviews and processing essential clinical trial documents in accordance with SOPs and regulatory standards. You will collaborate with project teams to ensure document accuracy and adherence to industry best practices.
Clinical Scientist - US - Remote
Worldwide Clinical Trials
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Full Time
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3 months ago
Worldwide Clinical Trials
The Clinical Scientist leads the review and assessment of clinical oncology data to ensure quality, integrity, and regulatory compliance. They collaborate with cross-functional teams to interpret clinical findings, monitor safety events, and support the development of key regulatory deliverables.
Senior Project Manager - US - Remote
Worldwide Clinical Trials
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Full Time
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3 months ago
Worldwide Clinical Trials
The Senior Project Manager is responsible for the end-to-end coordination and management of clinical trials from start-up to closeout. They oversee the technical, financial, and operational aspects of projects to ensure deliverables meet quality, time, and cost expectations.
Senior Associate I, TMF Operations - UK - Remote
Worldwide Clinical Trials
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Full Time
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3 months ago
Worldwide Clinical Trials
The Senior Associate will perform RMC lead activities for studies, including TMF set-up, maintenance, and coordination between project teams and eTMF administrators. They will also oversee quality control processes, monitor TMF metrics and KPIs, and provide support during regulatory and sponsor audits.
Clinical Research Associate - Italy - Remote
Worldwide Clinical Trials
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Full Time
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3 months ago
Worldwide Clinical Trials
Manage research activities at clinical sites, including study start-up, site training, and maintenance. Ensure compliance with regulatory requirements and oversee the collection of data and safety reporting throughout the study lifecycle.
Senior Clinical Research Associate - Oncology - Brazil - Remote
Worldwide Clinical Trials
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Full Time
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3 months ago
Worldwide Clinical Trials
The Senior Clinical Research Associate is responsible for managing research activities at clinical sites, including study start-up, site training, and maintenance. They ensure compliance with regulatory requirements and safety reporting while overseeing observational and non-interventional studies.
Vice President, Business Development - U.S. West Coast - Remote
Worldwide Clinical Trials
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Full Time
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3 months ago
Worldwide Clinical Trials
The Vice President of Business Development leads a team of account directors to drive sales targets and execute sponsor engagement strategies. This role is responsible for mentoring staff, managing performance, and collaborating with internal stakeholders to support the company's growth in the CRO market.
Director of Clinical Projects, Clinical Assessment Technologies - Europe - Remote
Worldwide Clinical Trials
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Full Time
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3 months ago
Worldwide Clinical Trials
The Director will engage with senior management to establish strategic department initiatives and drive business development activities for Clinical Assessment Technologies. They are also responsible for overseeing the development of assessment training content and ensuring all materials meet protocol and regulatory requirements.
Associate II, Pharmacovigilance - Brazil - Remote
Worldwide Clinical Trials
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Full Time
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3 months ago
Worldwide Clinical Trials
The Associate II is responsible for the collection, processing, evaluation, and reporting of Serious Adverse Event data in accordance with regulatory guidelines and SOPs. They also serve as the Lead PV Associate for studies, authoring safety management plans and performing quality control on safety information.
Consultant, Clinician -Clinical Assessment Technologies- Europe- Remote
Worldwide Clinical Trials
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Full Time
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3 months ago
Worldwide Clinical Trials
The consultant will conduct remote psychiatric patient interviews for clinical trials and provide training on assessment technologies. They are responsible for preparing scoring rationales and ensuring accurate data entry following each interview.
Senior Director, Business Partner
Worldwide Clinical Trials
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Full Time
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3 months ago
Worldwide Clinical Trials
The Senior Director, Business Partner will provide strategic HR leadership and support to a key business area, partnering with leaders to drive change management initiatives. They will also manage talent planning, employee engagement programs, and ensure compliance with HR policies and legal requirements.
Site Activation Specialist - Japan - Remote
Worldwide Clinical Trials
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Full Time
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4 months ago
Worldwide Clinical Trials
The specialist will track study-specific site regulatory documents, follow up on necessary actions, and support the development and review of country/site-specific informed consent forms. Responsibilities also include maintaining communication with sites for timely start-up activities and collecting/reviewing essential regulatory documents.
Sales Development Account Manager
Worldwide Clinical Trials
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Full Time
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4 months ago
Worldwide Clinical Trials
The Sales Development Account Manager engages with prospective clients and internal stakeholders to build an effective new business pipeline, partnering with Business Development to achieve territory targets and goals. Key tasks include sourcing new sales opportunities through lead qualification and outbound prospecting, maintaining the prospect database, and achieving lead generation goals.
Director, Business Development
Worldwide Clinical Trials
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Full Time
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4 months ago
Worldwide Clinical Trials
The Director of Business Development will achieve individual revenue and sales objectives by proactively communicating and selling Worldwide Clinical Trials' late-phase services to assigned clients. This role involves connecting the Worldwide team to established networks, identifying new leads for Phase II-IV business, and developing growth and retention strategies for the client base.
Senior Clinical Research Associate - Japan - Remote
Worldwide Clinical Trials
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Full Time
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4 months ago
Worldwide Clinical Trials
The role is responsible for managing research activities at sites, predominantly registries and non-interventional studies, covering all stages from site identification and start-up to maintenance and close-out. Key tasks include conducting Study Initiation Visits (SIVs), ensuring compliance with informed consent, safety reporting, and adhering to all applicable regulatory requirements, mostly performed remotely.
Azure Data & Platform Engineer - Serbia - Remote
Worldwide Clinical Trials
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Full Time
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4 months ago
Worldwide Clinical Trials
The role involves leading the migration of SQL Server and PostgreSQL workloads to Azure SQL Database and Azure SQL Managed Instances, alongside designing, deploying, and supporting PaaS and DBaaS offerings in Azure. Responsibilities also include analyzing and consolidating database instances for optimization and implementing native Azure backup, replication, disaster recovery, and security configurations.
Senior Associate, Pharmacovigilance - Japan - Remote
Worldwide Clinical Trials
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Full Time
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5 months ago
Worldwide Clinical Trials
The role involves authoring Safety Management Plans for assigned studies, attending internal and client meetings, and reviewing incoming Serious Adverse Event (SAE) data for completeness and accuracy. Responsibilities also include performing data entry into the Safety Database, generating queries for missing information, and generating regulatory reports and safety submissions as required.
