Worldwide Clinical Trials

Associate II, TMF Operations - Europe - Remote

Worldwide Clinical Trials · Full Time · 2 days ago

🌎 Croatia, Georgia, Oman, Poland, Romania, Serbia, Spain, United Kingdom ⭐ 2-5 yrs exp 💼 Others

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.

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Clinical Research Associate II - Cardio - East Coast/Central (Remote)

Worldwide Clinical Trials · Full Time · 3 days ago

Worldwide Clinical Trials

🌎 United States 💵 $79500 - $158K per year ⭐ 2-5 yrs exp 💼 Healthcare

The 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 oversee data collection and safety reporting throughout the study lifecycle.

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Senior Clinical Research Associate - CNS - Midwest/Southeast (Remote)

Worldwide Clinical Trials · Full Time · 3 days ago

Worldwide Clinical Trials

🌎 United States 💵 $97000 - $193K per year ⭐ 5-10 yrs exp 💼 Healthcare

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.

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Senior Clinical Research Associate - Psychedelics - West Coast (Remote)

Worldwide Clinical Trials · Full Time · 3 days ago

Worldwide Clinical Trials

🌎 United States 💵 $97000 - $193K per year ⭐ 5-10 yrs exp 💼 Healthcare

The Senior Clinical Research Associate is responsible for managing research activities at clinical sites, including study start-up, site training, and ongoing maintenance. They ensure compliance with regulatory requirements and safety reporting while conducting study initiation visits.

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Senior Clinical Research Associate - Obesity - Central U.S. (Remote)

Worldwide Clinical Trials · Full Time · 3 days ago

Worldwide Clinical Trials

🌎 United States 💵 $97000 - $193K per year ⭐ 5-10 yrs exp 💼 Healthcare

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.

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Senior Clinical Research Associate - Obesity or Rare Disease - Central/East (Remote)

Worldwide Clinical Trials · Full Time · 3 days ago

Worldwide Clinical Trials

🌎 United States 💵 $97000 - $193K per year ⭐ 5-10 yrs exp 💼 Healthcare

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.

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Senior Clinical Research Associate - Psychedelics - Central U.S. (Remote)

Worldwide Clinical Trials · Full Time · 3 days ago

Worldwide Clinical Trials

🌎 United States 💵 $97000 - $193K per year ⭐ 5-10 yrs exp 💼 Healthcare

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.

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Senior Clinical Trial Manager - Oncology - U.S. (Remote)

Worldwide Clinical Trials · Full Time · 3 days ago

Worldwide Clinical Trials

🌎 United States 💵 $112K - $222K per year ⭐ 5-10 yrs exp 💼 Healthcare

Provide leadership and direction to clinical site management team members from study start through to closure. Serve as the primary point of contact for clinical monitoring and site activities while managing deliverables to meet study budgets.

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Sales Development Account Manager - Europe - Remote

Worldwide Clinical Trials · Full Time · 4 days ago

Worldwide Clinical Trials

🌎 France, Germany, Italy, Serbia, Spain ⭐ 2-5 yrs exp 💼 Sales

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.

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Senior Project Manager - Oncology - Japan (Remote)

Worldwide Clinical Trials · Full Time · 4 days ago

Worldwide Clinical Trials

🌎 Japan ⭐ 5-10 yrs exp 💼 Product

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.

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Site Activation Operations Director - Australia - Remote

Worldwide Clinical Trials · Full Time · 4 days ago

Worldwide Clinical Trials

🌎 Australia ⭐ 5-10 yrs exp 💼 Others

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.

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Grants Payments Data Analyst - Serbia/Bulgaria - Remote

Worldwide Clinical Trials · Full Time · 4 days ago

Worldwide Clinical Trials

🌎 Bulgaria, Serbia ⭐ 2-5 yrs exp 💼 Software Development

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.

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Clinical Systems Support Assistant - Fixed Term - Serbia/UK - Remote

Worldwide Clinical Trials · Full Time · 5 days ago

Worldwide Clinical Trials

🌎 Serbia, United Kingdom ⭐ 0-2 yrs exp 💼 Support

The role involves supporting clinical systems project associates with system maintenance, project communications, and tracking study deliverables. You will also provide first-line support for clinical systems and assist with training documentation and record retention.

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Vendor Contracts Manager III

Worldwide Clinical Trials · Full Time · 5 days ago

Worldwide Clinical Trials

🌎 United States 💵 $65500 - $130K per year ⭐ 2-5 yrs exp 💼 Others

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.

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Senior Legal Contract Manager

Worldwide Clinical Trials · Full Time · 5 days ago

Worldwide Clinical Trials

🌎 Mexico ⭐ 5-10 yrs exp 💼 Legal

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.

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Senior Associate I, TMF Operations Fix term

Worldwide Clinical Trials · Full Time · 5 days ago

Worldwide Clinical Trials

🌎 Argentina, Brazil, Mexico ⭐ 2-5 yrs exp 💼 Others

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.

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Associate I, TMF Operations

Worldwide Clinical Trials · Full Time · 5 days ago

Worldwide Clinical Trials

🌎 Argentina ⭐ 0-2 yrs exp 💼 Others

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.

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Senior Clinical Research Associate - CNS/Psychiatry - West Coast (Remote)

Worldwide Clinical Trials · Full Time · 5 days ago

Worldwide Clinical Trials

🌎 United States 💵 $97000 - $193K per year ⭐ 5-10 yrs exp 💼 Healthcare

The Senior Clinical Research Associate manages research activities at clinical sites, including study start-up, site training, and maintenance. They ensure regulatory compliance and safety reporting while conducting study initiation visits and overseeing site activities.

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Site Contracts Lead - Europe - Remote

Worldwide Clinical Trials · Full Time · 6 days ago

Worldwide Clinical Trials

🌎 Bulgaria, Croatia, Hungary, Italy, Oman, Poland, Romania, Serbia, Spain, United Kingdom ⭐ 5-10 yrs exp 💼 Others

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.

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Senior Clinical Research Associate - CNS - Midwest (Remote)

Worldwide Clinical Trials · Full Time · 6 days ago

Worldwide Clinical Trials

🌎 United States 💵 $97000 - $193K per year ⭐ 5-10 yrs exp 💼 Healthcare

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.

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Senior Clinical Research Associate - Oncology - Northeast/Midwest (Remote)

Worldwide Clinical Trials · Full Time · 6 days ago

Worldwide Clinical Trials

🌎 United States 💵 $97000 - $193K per year ⭐ 5-10 yrs exp 💼 Healthcare

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.

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Senior Clinical Research Associate - Oncology - Florida (Remote)

Worldwide Clinical Trials · Full Time · 6 days ago

Worldwide Clinical Trials

🌎 United States 💵 $97000 - $193K per year ⭐ 5-10 yrs exp 💼 Healthcare

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.

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In-House Clinical Research Associate - Spain

Worldwide Clinical Trials · Full Time · 7 days ago

Worldwide Clinical Trials

🌎 Spain ⭐ 0-2 yrs exp 💼 Healthcare

Ensure the quality and timely submission of study site data and safety reporting. Manage regulatory documentation, ethical submissions, and Trial Master File updates while performing site feasibility studies.

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In-House Clinical Research Associate - Poland or Serbia

Worldwide Clinical Trials · Full Time · 7 days ago

Worldwide Clinical Trials

🌎 Poland, Serbia ⭐ 0-2 yrs exp 💼 Healthcare

Ensure the quality and timely submission of study site data and safety reporting. Manage regulatory documentation, ethical submissions, and Trial Master File updates while performing site feasibility studies.

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Operations Finance Data & Reporting Analyst I - Bulgaria - Remote

Worldwide Clinical Trials · Full Time · 7 days ago

Worldwide Clinical Trials

🌎 Bulgaria ⭐ 0-2 yrs exp 💼 Finance

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.

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Senior Clinical Research Associate - Oncology, Rare Disease - Japan

Worldwide Clinical Trials · Full Time · 7 days ago

Worldwide Clinical Trials

🌎 Sweden ⭐ 2-5 yrs exp 💼 Healthcare

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.

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Clinical Trials Associate

Worldwide Clinical Trials · Full Time · 10 days ago

Worldwide Clinical Trials

🌎 Argentina ⭐ 0-2 yrs exp 💼 Healthcare

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 clinical trial documentation and the trial master file.

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Senior Clinical Data Manager

Worldwide Clinical Trials · Full Time · 10 days ago

Worldwide Clinical Trials

🌎 United States 💵 $79000 - $157K per year ⭐ 5-10 yrs exp 💼 Healthcare

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.

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Senior Clinical Research Associate

Worldwide Clinical Trials · Full Time · 11 days ago

Worldwide Clinical Trials

🌎 Brazil ⭐ 2-5 yrs exp 💼 Healthcare

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.

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Senior Clinical Research Associate - Psychiatry - West Coast (Remote)

Worldwide Clinical Trials · Full Time · 11 days ago

Worldwide Clinical Trials

🌎 United States 💵 $97000 - $193K per year ⭐ 5-10 yrs exp 💼 Healthcare

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.

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Senior Clinical Research Associate - Psychiatry - Central U.S. (Remote)

Worldwide Clinical Trials · Full Time · 11 days ago

Worldwide Clinical Trials

🌎 United States 💵 $97000 - $193K per year ⭐ 5-10 yrs exp 💼 Healthcare

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.

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Senior Clinical Research Associate - Psychiatry - East Coast (Remote)

Worldwide Clinical Trials · Full Time · 11 days ago

Worldwide Clinical Trials

🌎 United States 💵 $97000 - $193K per year ⭐ 5-10 yrs exp 💼 Healthcare

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.

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TMF Team Lead - EMEA/LATAM- Fixed term - Remote

Worldwide Clinical Trials · Full Time · 12 days ago

Worldwide Clinical Trials

🌎 Argentina, Brazil, Bulgaria, Croatia, Mexico, Oman, Poland, Romania, Serbia ⭐ 2-5 yrs exp 💼 Others

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.

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Associate Director, Project Management - Oncology - Europe - Remote

Worldwide Clinical Trials · Full Time · 12 days ago

Worldwide Clinical Trials

🌎 Bulgaria, Croatia, Hungary, Oman, Poland, Romania, Serbia, Spain, United Kingdom ⭐ 10+ yrs exp 💼 Product

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.

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Senior Clinical Research Associate - Oncology - Southeast/Mid-Atlantic (Remote)

Worldwide Clinical Trials · Full Time · 16 days ago

Worldwide Clinical Trials

🌎 United States 💵 $97000 - $193K per year ⭐ 5-10 yrs exp 💼 Healthcare

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.

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Senior Clinical Research Associate - CNS - Central U.S. (Remote)

Worldwide Clinical Trials · Full Time · 16 days ago

Worldwide Clinical Trials

🌎 United States 💵 $97000 - $193K per year ⭐ 5-10 yrs exp 💼 Healthcare

Manage research activities at clinical sites, including site identification, start-up activities, and study maintenance. Conduct study initiation visits and ensure compliance with informed consent and regulatory requirements.

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Senior Clinical Data Manager

Worldwide Clinical Trials · Full Time · 17 days ago

Worldwide Clinical Trials

🌎 United States 💵 $79000 - $157K per year ⭐ 5-10 yrs exp 💼 Healthcare

Oversee and lead data management services across multiple complex global projects from start-up to close-out. Ensure accurate trial documentation, effective UAT, and timely database locks while managing project budgets and risks.

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Senior Biostatistician

Worldwide Clinical Trials · Full Time · 17 days ago

Worldwide Clinical Trials

🌎 United States 💵 $87500 - $173K per year ⭐ 5-10 yrs exp 💼 Healthcare

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.

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Senior Proposal Associate - Writing - US - Remote

Worldwide Clinical Trials · Full Time · 17 days ago

Worldwide Clinical Trials

🌎 United States 💵 $65000 - $129K per year ⭐ 2-5 yrs exp 💼 Others

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.

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Senior Clinical Research Associate - Rare CNS - Florida (Remote)

Worldwide Clinical Trials · Full Time · 18 days ago

Worldwide Clinical Trials

🌎 United States 💵 $97000 - $193K per year ⭐ 5-10 yrs exp 💼 Healthcare

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.

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Senior Clinical Research Associate - CNS - Southeast/MidAtlantic (Remote)

Worldwide Clinical Trials · Full Time · 18 days ago

Worldwide Clinical Trials

🌎 United States 💵 $97000 - $193K per year ⭐ 5-10 yrs exp 💼 Healthcare

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.

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Senior Clinical Research Associate - Oncology - Northern Midwest (Remote)

Worldwide Clinical Trials · Full Time · 18 days ago

Worldwide Clinical Trials

🌎 United States 💵 $97000 - $193K per year ⭐ 5-10 yrs exp 💼 Healthcare

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.

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Senior Clinical Research Associate - CNS - Southeast (Remote)

Worldwide Clinical Trials · Full Time · 18 days ago

Worldwide Clinical Trials

🌎 United States 💵 $97000 - $193K per year ⭐ 5-10 yrs exp 💼 Healthcare

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.

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Senior Clinical Research Associate - CNS/Rare Disease - Midwest (Remote)

Worldwide Clinical Trials · Full Time · 18 days ago

Worldwide Clinical Trials

🌎 United States 💵 $97000 - $193K per year ⭐ 5-10 yrs exp 💼 Healthcare

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.

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Senior Clinical Research Associate - US - Oncology

Worldwide Clinical Trials · Full Time · 18 days ago

Worldwide Clinical Trials

🌎 United States 💵 $97000 - $193K per year ⭐ 5-10 yrs exp 💼 Healthcare

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.

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Contract Manager - Bulgaria/Romania - Remote

Worldwide Clinical Trials · Full Time · 19 days ago

Worldwide Clinical Trials

🌎 Norway ⭐ 2-5 yrs exp 💼 Legal

Manage the full life cycle of sponsor contracts and change orders, including drafting budgets and scopes of work. Collaborate with cross-functional departments to negotiate and finalize legal, financial, and operational terms with sponsors.

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Regulatory Affairs Specialist- Belgian Dutch speaker- Remote

Worldwide Clinical Trials · Full Time · 19 days ago

Worldwide Clinical Trials

🌎 Belgium, France, Netherlands ⭐ 2-5 yrs exp 💼 Legal

The role involves planning and submitting regulatory dossiers and coordinating with ethics committees to ensure clinical trial compliance. It also requires maintaining country-specific labeling and patient information while providing strategic regulatory advice.

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Market Intelligence Analyst

Worldwide Clinical Trials · Full Time · 19 days ago

Worldwide Clinical Trials

🌎 Ireland, United Kingdom ⭐ 2-5 yrs exp 💼 Marketing

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.

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Pharmacovigilance Specialist - US - Remote

Worldwide Clinical Trials · Full Time · 19 days ago

Worldwide Clinical Trials

🌎 Brazil, Mexico, Serbia, United Kingdom, United States 💵 $50000 - $99000 per year ⭐ 0-2 yrs exp 💼 Others

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.

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Senior Clinical Research Associate - Oncology, Hematology - France

Worldwide Clinical Trials · Full Time · 20 days ago

Worldwide Clinical Trials

🌎 France ⭐ 2-5 yrs exp 💼 Healthcare

The role is responsible for managing the full lifecycle of clinical sites, including qualification, monitoring, and close-out visits. It also involves mentoring junior CRAs and ensuring data veracity and protocol compliance.

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Senior Statistician

Worldwide Clinical Trials · Full Time · 21 days ago

Worldwide Clinical Trials

🌎 United Kingdom, United States 💵 $87500 - $173K per year ⭐ 2-5 yrs exp 💼 Software Development

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.

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Medical Director, Medical Affairs - US - Remote

Worldwide Clinical Trials · Full Time · 23 days ago

Worldwide Clinical Trials

🌎 United States 💵 $134K - $267K per year ⭐ 2-5 yrs exp 💼 Healthcare

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.

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Senior Manager, Clinical Operations Site Management (Franchise Lead) - Europe - Remote

Worldwide Clinical Trials · Full Time · 23 days ago

Worldwide Clinical Trials

🌎 United Kingdom ⭐ 10+ yrs exp 💼 Healthcare

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.

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Project Manager - Oncology - US/Canada - Remote

Worldwide Clinical Trials · Full Time · 24 days ago

Worldwide Clinical Trials

🌎 Canada, United States 💵 $112K - $222K per year ⭐ 5-10 yrs exp 💼 Product

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.

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Senior Clinical Research Associate - Rare CNS - Southeast/Mid-Atlantic (Remote)

Worldwide Clinical Trials · Full Time · 24 days ago

Worldwide Clinical Trials

🌎 United States 💵 $97000 - $193K per year ⭐ 5-10 yrs exp 💼 Healthcare

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.

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Senior Clinical Research Associate - CNS/Rare Disease - Central U.S. (Remote)

Worldwide Clinical Trials · Full Time · 24 days ago

Worldwide Clinical Trials

🌎 United States 💵 $97000 - $193K per year ⭐ 5-10 yrs exp 💼 Healthcare

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.

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Senior Clinical Research Associate - Rare CNS - Southeast/Mid-Atlantic (Remote)

Worldwide Clinical Trials · Full Time · 24 days ago

Worldwide Clinical Trials

🌎 United States 💵 $97000 - $193K per year ⭐ 5-10 yrs exp 💼 Healthcare

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.

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Senior Clinical Research Associate - Oncology/Rare Disease - Texas (Remote)

Worldwide Clinical Trials · Full Time · 24 days ago

Worldwide Clinical Trials

🌎 United States 💵 $97000 - $193K per year ⭐ 5-10 yrs exp 💼 Healthcare

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.

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Project Manager - Oncology - Australia - Remote

Worldwide Clinical Trials · Full Time · 25 days ago

Worldwide Clinical Trials

🌎 Australia ⭐ 5-10 yrs exp 💼 Product

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.

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Clinical Research Associate - Neurology, Oncology - Germany

Worldwide Clinical Trials · Full Time · 25 days ago

Worldwide Clinical Trials

🌎 Germany ⭐ 2-5 yrs exp 💼 Healthcare

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.

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Clinical Research Associate - Oncology, Hematology - Italy

Worldwide Clinical Trials · Full Time · 25 days ago

Worldwide Clinical Trials

🌎 Italy ⭐ 2-5 yrs exp 💼 Healthcare

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.

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Senior Clinical Research Associate (Bilingual) - Oncology - Canada (Remote)

Worldwide Clinical Trials · Full Time · 25 days ago

Worldwide Clinical Trials

🌎 Canada ⭐ 5-10 yrs exp 💼 Healthcare

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.

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Senior Clinical Research Associate - Oncology - Brazil - Remote

Worldwide Clinical Trials · Full Time · 25 days ago

Worldwide Clinical Trials

🌎 Brazil ⭐ 5-10 yrs exp 💼 Healthcare

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.

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