71 matching jobs for “CRA (Level II)”

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Exact titles rank first, then title variations and keywords in descriptions. These labels aren't qualification scores. Without keywords, recently added jobs appear first.

Bristol-Myers Squibb

Clinical Trial Monitor I/ II

Beijing - CN +1 location

Full time
Temporary

Added Oct 15, 2026

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Thermo Fisher Scientific

FSP Country Approval Specialist II

Remote, Denmark

… path for site activation. • Achieves PPD’s target cycle times for site. • May work with the start-up CRA(s) to prepare the regulatory compliance review packages, as applicable. • May develop country specific …

Added Oct 16, 2026

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Thermo Fisher Scientific

FSP Clinical Research Associate II

Remote, Mexico

… Performs additional study tasks as assigned by CTM (e.g. trip report review, newsletter creation, lead CRA team calls etc). Facilitates effective communication between investigative sites, the client company and …

Added Oct 16, 2026

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Pfizer

Senior Clinical Research Associate I & II (Multiple positions)

Madrid, Spain

Full time
Regular

… Clinical Research Associates and Senior Clinical Research Associates I, as assigned Serve as an SME for CRA-related processes Participate in or lead global, regional or local working groups/process improvement …

Added Oct 16, 2026

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IQVIA Holdings

Clinical Research Associate II - Sponsor dedicated - Belgium - Home based (m/w/d)

Zaventem, Belgium

… SOP’s, creating more continuity for both parties. Our models offer excellent opportunities for experienced CRA’s to expand their knowledge and skills. IQVIA Belgium are currently seeking motivated Clinical Research …

Added Oct 15, 2026

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IQVIA Holdings

Clinical Research Associate II - Sponsor dedicated - Netherlands - Home based (m/w/d)

Amsterdam, The Netherlands

… SOP’s, creating more continuity for both parties. Our models offer excellent opportunities for experienced CRA’s to expand their knowledge and skills. IQVIA Netherlands are currently seeking motivated Clinical Research …

Added Oct 15, 2026

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IQVIA Holdings

Clinical Research Associate 1 or 2 (m/w/d), Single Sponsor

Frankfurt, Hesse, Germany

Added Oct 15, 2026

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Thermo Fisher Scientific

Global Study Manager - FSP - EMEA

Remote, Bulgaria +2 locations

… Plan Study Delivery Plan TMF Quality Strategy Document DCT Set Up Vendors Oversight Plan Investigator/CRA Meeting Set Up & associated training Recruitment Tracking Budget tracking eTMF filing and Vendor Set Up and …

Added Oct 16, 2026

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Thermo Fisher Scientific

Global Study Manager - FSP - UK - PACT/MAP experience

Remote, United Kingdom

Added Oct 16, 2026

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Merck (MSD)

(Associate) Clinical Operations Manager

GRC - Attica - Alimos

… You'll coordinate and liaise with Clinical Research Managers (CRM), CTCs, Clinical Research Associates (CRA), and other departments to ensure country deliverables are achieved. Collaborate closely with Headquarters …

Added Oct 15, 2026

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Thermo Fisher Scientific

Senior Clinical Research Associate

Sydney, Australia

… is safe or helping find cures for cancer. About the Role: Join Us as a Senior Clinical Research Associate (Level II) – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 …

Added Oct 16, 2026

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Bristol-Myers Squibb

Clinical Trial Monitor I/ II

Beijing - CN +1 more

Full time
Temporary

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About this opportunity

Original employer description

At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it.

The Clinical Research Associate (CRA) is a primary point of contact at the site level for both internal and external stakeholders, responsible for study startup at site， overseeing the quality, integrity and compliance of clinical trial sites in accordance with the protocol, Standard Operating Procedures (SOPs), International Council for Harmonization (ICH) Guideline for Good Clinical Practice (GCP), and applicable regulatory requirements.

We hire for skills and capabilities, not just credentials – if this role excites you, but doesn’t perfectly match your resume, we encourage you to apply anyway.

How We Work

Where you work matters – because collaboration, innovation and patient impact happen in many settings. Our roles are structured across four work models: site-essential, site-by-design, field-based and remote-by-design. The model assigned to this role is based on its core responsibilities. Learn more at https://careers.bms.com/ways-of-working.

Supporting People with Disabilities

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to [email protected]. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

Candidate Rights

BMS will consider qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

For roles based in Los Angeles County only: If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/

Data Protection

We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection.

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

If this posting is missing required information required by local law or incorrect, contact BMS at [email protected] with the Job Title and Requisition number. Do not send application-related inquiries to this email. To check your application status, please login to your Candidate Home Account.

R1605930 : Clinical Trial Monitor I/ II

Why this result? · Employer labels

Keywords also found in description

Clinical Development
Fixed Term (Fixed Term)
Full time

Location reference: GeoNames (CC BY 4.0), normalized by Referizz.