The Regulatory Affairs Specialist will plan, compile, and submit regulatory documentation while ensuring compliance with evolving global regulations. They will also act as a key point of contact for regulatory authorities and provide strategic guidance to project teams.
The Senior Clinical Research Associate manages research activities at clinical sites, including study start-up, site training, and maintenance. They are responsible for ensuring regulatory compliance, managing informed consent, and overseeing safety-related event reporting throughout the study lifecycle.
The Site Contracts Specialist is responsible for drafting, negotiating, and finalizing clinical trial site agreements and budgets. They also liaise with legal, data privacy, and study teams to ensure all contractual documentation is executed and tracked accurately.
The Senior Associate will manage complex TMF activities, oversee quality control processes, and ensure compliance with regulatory standards. They will also act as a subject matter expert, collaborating with project teams and sponsors to maintain essential clinical trial records.
The RTSM Specialist provides project management oversight for RTSM study lifecycles, ensuring deliverables meet SOP standards and timelines. They act as the primary point of contact for stakeholders and manage study design, budget, and system validation activities.
Develop, test, and execute SAS programs to produce CDISC SDTM and ADaM datasets, tables, figures, and listings. Serve as a programming project lead for medium complexity studies while ensuring data quality and regulatory standards are met.
The Clinical Trial Manager is responsible for leading clinical study site management activities and coordinating a team of clinical staff within a geographic region. They ensure site qualification, initiation, monitoring, and close-out activities are conducted in compliance with study protocols and standard operating procedures.
The Senior Project Manager is responsible for the overall 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 customer expectations for time, quality, and cost.
The specialist serves as the primary point of contact for regulatory submissions, site activation, and maintenance activities for assigned clinical projects. They are responsible for planning, tracking essential documents, and ensuring compliance with ICH GCP and local regulatory requirements.
The Site Activation Manager is responsible for coordinating and overseeing site identification, essential document collection, and contract status for clinical trials. They ensure all start-up activities are completed on time and within budget while maintaining compliance with GCP and local regulations.
The Clinical Trials Associate provides administrative and project tracking support to the clinical project team to ensure tasks are completed accurately. Responsibilities include maintaining project documentation, managing system access, and coordinating project-related meetings.
The Project Manager is responsible for the end-to-end coordination and management of clinical trials from startup through closeout. They lead cross-functional teams to ensure project deliverables meet time, quality, and cost expectations while implementing rescue strategies when necessary.
The Medical Director serves as the Global Lead Medical Monitor for clinical trials, providing therapeutic expertise and protocol-specific training to project teams. They also contribute medical input to clinical development programs and support business development activities through proposal generation and sponsor meetings.
The Clinical Trials Associate provides administrative and project tracking support to the clinical project team to ensure tasks are performed accurately. Responsibilities include managing system access, maintaining project documentation, and performing quality audits on trial files.
The Project Manager is responsible for the end-to-end coordination and management of clinical trials from startup through closeout. They lead cross-functional teams to ensure project deliverables meet time, quality, and cost expectations while implementing contingency plans as needed.
The Clinical Trials Associate provides administrative and project tracking support to the clinical project team to ensure tasks are performed accurately. Responsibilities include managing system access, maintaining project documentation, and assisting with trial master file submissions.
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 quality, time, and cost expectations.
The specialist will manage, compile, and submit regulatory documentation while ensuring compliance with ICH GCP and local requirements. They will also act as a liaison for translation reviews and maintain country-specific patient information and labeling.
The Clinical Data Associate assists the Data Manager with data cleaning, trial documentation, and database verification. They are also responsible for user registration in EDC/CTMS systems and reconciling data from external sources.
The Principal Statistician will design clinical trials, write Statistical Analysis Plans, and provide statistical leadership across various therapeutic areas. They will also develop and validate SAS programs for statistical analysis while ensuring compliance with regulatory standards and sponsor requirements.
The Senior Clinical Research Associate manages research activities at clinical sites, including study start-up, site training, and maintenance. They ensure compliance with regulatory requirements and safety reporting while conducting study initiation visits.
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, manage informed consent processes, and oversee safety-related event reporting.
The Site Activation Manager is responsible for the end-to-end management and delivery of site activation activities within an assigned therapeutic area. This includes coordinating site identification, managing essential document collection, and ensuring all processes comply with GCP and local regulations.
The Senior Biostatistician manages statistical project support and provides expert consultancy for clinical trials, including study design and analysis plans. They are responsible for developing SAS programs, validating datasets, and ensuring compliance with regulatory standards like ICH and FDA.
The Manager, Regulatory Affairs provides expert regulatory guidance throughout the drug development cycle and oversees the compilation and submission of regulatory dossiers. They are also responsible for mentoring junior staff, managing departmental work practices, and ensuring compliance with international regulations.
The Director serves as the single point of contact for a portfolio of EPMO projects, driving strategic planning, problem-solving, and value realization. They also coach project leaders, facilitate executive governance, and champion the integration of AI into project methodologies.
The specialist will analyze PSC workflows to identify inefficiencies and implement automation solutions to improve operational performance. They will also translate complex data into actionable insights and KPIs to support leadership decision-making.
The Investigator Grants Specialist is responsible for the development, delivery, and maintenance of investigator grants during both the bidding and template development phases. They also provide strategic advice to internal departments regarding forecasting and risk mitigation for clinical trial budgets.
The Contract Manager is responsible for the full life cycle of sponsor contracts and change orders, including drafting, budget preparation, and negotiation. They collaborate with internal departments such as Legal, Finance, and Operations to ensure compliance and accurate project scope definition.
The Clinical Trials Associate provides administrative and project tracking support to the clinical project team to ensure tasks are completed accurately. They are responsible for maintaining project documentation, managing system access, and performing quality audits on trial-related files.
The specialist will manage planned and unplanned quality management document deviations and support stakeholder training on QMS tools. They are also responsible for conducting quarterly trend analysis and reporting KPIs to the relevant governance committees.
The Contract Manager is responsible for the full life cycle of sponsor contracts, including drafting budgets, scopes of work, and legal terms. They will collaborate with cross-functional departments to negotiate study budgets and finalize project timelines and costs.
The role involves processing, reviewing, and maintaining Trial Master File (TMF) documents in accordance with SOPs and regulatory standards. You will perform quality control reviews and collaborate with project teams to ensure document accuracy and compliance.
The Senior Clinical Trial Manager oversees clinical study site management activities and leads a team of clinical staff on complex global studies. They are responsible for ensuring site qualification, initiation, monitoring, and close-out activities while maintaining data quality and project timelines.
The Grants Payments Data Analyst will build and maintain forecasting models for clinical site payments while collaborating with cross-functional teams to ensure financial accuracy. They are responsible for creating client-ready deliverables, performing variance analysis, and ensuring compliance with audit requirements.
The Clinical Research Associate is responsible for site qualification, initiation, monitoring, and study close-out visits to ensure protocol adherence and data integrity. They also provide mentoring to less experienced staff and maintain accurate documentation for the Trial Master File.
The Senior Clinical Research Associate manages research activities at clinical sites, including study start-up, site training, and maintenance. They are responsible for ensuring regulatory compliance, managing safety reporting, and overseeing site activities throughout the study lifecycle.
The In-House Clinical Research Associate II is responsible for managing clinical study sites in accordance with GCPs and regulatory requirements. They provide support to project teams, maintain study documentation, and assist with remote monitoring and data management tasks.
The Vice President of Corporate Development will lead the company's global inorganic growth strategy, including mergers, acquisitions, and strategic partnerships. They will manage end-to-end deal execution and coordinate cross-functional teams to ensure successful post-merger integration and value creation.
The role involves processing, reviewing, and maintaining essential clinical trial documents in accordance with SOPs and regulatory standards. You will perform quality control reviews and collaborate with project teams to ensure document accuracy and compliance.
The Executive Assistant provides high-level administrative support to the BU Head and the Internal Medicine Team, including complex calendar management and travel coordination. They are responsible for managing correspondence, organizing meetings across global time zones, and ensuring compliance within the business unit.
The Senior CRA is responsible for site qualification, initiation, monitoring, and close-out visits to ensure protocol adherence and data integrity. They also provide mentorship to less experienced staff and ensure compliance with regulatory and trial master file documentation.
The Senior Clinical Trial Liaison will establish and maintain relationships with key opinion leaders and site staff to ensure the quality and feasibility of oncology clinical trials. They will provide strategic input on protocol development, site selection, and business development activities to support internal and external project teams.
The Patient and Site Solutions Enablement Project Manager leads the implementation and adoption of new data and technology processes within the clinical research feasibility department. This role acts as a key conduit between functional SMEs, vendors, and technical teams to ensure business requirements and ROI expectations are met.
The Director will oversee the delivery of clinical projects within cost, time, and quality requirements while providing direct supervision and mentoring to project managers. They will also collaborate with the Business Development team on proposals and contribute to the continuous improvement of business processes.
The Site Identification and Relationship Manager will lead post-award site identification strategies, including feasibility assessments and outreach coordination. They are also responsible for training assigned resources and overseeing Site Activation Specialist support activities.
The Site Identification and Relationship Manager will lead post-award site identification strategies, including feasibility management and outreach coordination. They are also responsible for training assigned resources and overseeing Site Activation Specialist support activities.
The Regulatory Affairs Specialist will plan, compile, and submit regulatory documentation while ensuring compliance with evolving global regulations. They will also act as a key point of contact for regulatory intelligence and provide strategic advice to project teams regarding submission processes.
The role involves processing, maintaining, and archiving essential clinical trial documents while performing TMF quality control reviews. You will collaborate with project teams to ensure adherence to regulatory standards and industry best practices.
The Senior Clinical Research Associate manages research activities at clinical sites, including study start-up, site training, and maintenance. They ensure regulatory compliance and data integrity while overseeing site performance throughout the study lifecycle.
The Senior Clinical Research Associate manages research activities at clinical sites, including study start-up, site training, and maintenance. They are responsible for ensuring regulatory compliance, managing safety reporting, and conducting study initiation visits.
The Senior Clinical Research Associate is responsible for managing research activities at clinical sites, including study start-up, site training, and regulatory compliance. They will conduct study initiation visits and oversee site performance throughout the duration of the clinical trials.
The Senior Clinical Research Associate manages research activities at clinical sites, including study start-up, site training, and maintenance. They are responsible for ensuring regulatory compliance, managing informed consent, and overseeing safety reporting throughout the study lifecycle.
The Sales Development Account Manager is responsible for sourcing new sales opportunities through inbound lead qualification and outbound prospecting. They will collaborate with Business Development partners to manage territories, set appointments, and drive leads through the early stages of the sales process.
The Senior Project Manager is responsible for the overall 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 customer expectations.
The Site Activation Operations Director is responsible for the operational and financial delivery of end-to-end site activation, including resource management and process improvement. They lead regulatory intelligence initiatives, manage departmental metrics, and supervise the Site Activation Operations team to ensure alignment with corporate strategy.
The Grants Payments Data Analyst is responsible for developing and maintaining financial forecast models for clinical site payments outside of Medidata Payments. They will collaborate with cross-functional teams to ensure accurate reporting, audit compliance, and the delivery of financial data for client deliverables.
The Vendor Contracts Manager is responsible for the full life cycle of vendor contracts, including drafting, reviewing, and negotiating agreements. They also focus on process improvement and risk mitigation to ensure efficient contract administration and compliance with company policies.
The Senior Legal Contract Manager is responsible for independently reviewing, redlining, and negotiating sponsor-facing legal and commercial contracts. They will manage the full contract lifecycle while collaborating with internal stakeholders to ensure alignment on business, legal, and operational requirements.
The Senior Associate will manage complex TMF studies, provide subject matter expertise, and oversee quality control processes to ensure regulatory compliance. They will also prepare TMF performance metrics and support project teams during audits and sponsor interactions.
The Associate will process, review, and resolve Trial Master File (TMF) documents while ensuring compliance with SOPs and industry regulations. They will also provide administrative support to the RMC Lead, including maintaining quality control checklists and tracking study documentation.
Serve as the primary point of contact for project teams and sponsors regarding study site contracting activities. Lead and mentor site contracts specialists while negotiating and finalizing clinical trial agreements and budgets.
Manage research activities at clinical sites, including site identification, start-up, and close-out activities. Conduct study initiation visits and ensure compliance with informed consent and regulatory requirements.
The analyst will prepare financial metrics and reports for internal management while enhancing business tools to automate processes. Key duties include project setup, ERP data integrity maintenance, and managing the timekeeping and billing processes.
The CRA is responsible for managing the full lifecycle of study sites, including qualification, initiation, monitoring, and close-out. They ensure protocol adherence, verify source documents for data veracity, and provide guidance to site staff and junior CRAs.
Oversee and lead data management services across multiple complex global clinical projects from start-up to closeout. This includes preparing trial documentation, managing database locks, and coordinating with internal departments and sponsors.
Manage research activities at clinical sites, including site identification, start-up, and close-down. Conduct study initiation visits and ensure compliance with informed consent and safety reporting requirements.
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.
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.
The Team Lead is responsible for maintaining Trial Master Files inspection readiness in compliance with SOPs, ALCOA principles, and industry regulations. They drive the delivery of project objectives and oversee TMF services for multiple studies while managing risks and KPIs.
Accountable for directing multiple oncology projects simultaneously to ensure delivery within cost, time, and quality requirements. Collaborates with cross-functional leadership to improve business processes and supports proposal development for new clients.
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.
Independently manages statistical project support and provides expert consultancy for clinical trial designs and analysis plans. Develops and runs SAS programs for data reporting while ensuring compliance with regulatory standards like FDA and ICH.
Lead the writing, coordination, and presentation of robust proposals for assigned projects. Collaborate with Account Directors and subject matter experts to manage the proposal development process and ensure accurate service offerings.
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.
Manage research activities at clinical sites, including site identification, start-up, and close-out activities. Conduct study initiation visits and ensure compliance with informed consent and safety reporting requirements.
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.
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.
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.
The analyst is responsible for assessing core therapeutic markets and providing data-driven analysis to guide decisions on new market entries. Key tasks include maintaining market models, tracking drug compounds, and providing presentations to internal stakeholders.
Responsible for the collection, processing, evaluation, and reporting of Serious Adverse Event (SAE) data according to regulatory guidelines. The role involves authoring Safety Management Plans and performing quality control on safety data processed by other associates.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
