Associate Manager, CDM – Bristol Myers Squibb

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Working with Us

Challenging, meaningful, and life‑changing. Working at Bristol Myers Squibb is anything but ordinary. Each day brings unique, transformative work—from optimizing production lines to breakthroughs in cell therapy. You’ll grow through opportunities unlike any other, collaborating with high‑achieving teams and advancing patient care.

We value balance and flexibility, offering competitive benefits, services, and programs to support personal and professional goals. Read more.

Position Summary

The Associate Manager, Clinical Data Management is a full‑time, office‑based role with flexibility to work remotely up to 50% of the time. The role reports to a line manager within CDM and is essential to completing end‑to‑end data management tasks on assigned studies across therapeutic areas.

Position Responsibilities

Study Startup

• Draft EDC build timeline in collaboration with the Data Management Lead.
• Perform database build tasks and create specifications for Database and Edit Checks.
• Create test scripts and complete test data entry/UAT for Coding, Site Payment, Safety Gateway.
• Collaborate with the Data Management Lead to facilitate startup meetings, including EDC build kick‑off, Interactive eCRF Build and IRMs for database and Edit checks.
• Create and finalize study documents such as the Data Quality Management Plan, eCRF completion Instructions, and Protocol Data Review Plan following study team review.
• Ensure all startup documents are completed per SOP and filed in eTMF according to the master plan.

Study Conduct

• Plan and execute post‑production/migration for the study, if applicable.
• Coordinate with Clinical Data Managers for data review activities.
• Coordinate with external data vendors for any escalations related to vendor data.
• Support Clean Patient Group delivery along with Clinical Data Management staff.
• Update study documents as needed during the conduct.
• Support Data Management Lead in conducting Data Quality Review meetings.
• Provide Data Health Metrics to the Data Management Lead as requested.

Study Closeout

• Support the Data Management Lead in planning and executing database lock activities.
• Perform post‑lock activities as needed.

Project Management

• Support the Data Management Lead in project management tasks to ensure study delivery successfully within timelines and quality standards.

Documentation

• File appropriate documents in eTMF per the master plan.

Training and Mentorship

• Provide training and mentorship to junior CDM staff.

Requirements

• Bachelors Degree required. Preferred fields: Life sciences, Pharmacy, or related areas.
• 6+ years of experience managing end‑to‑end Clinical Data Management tasks.
• Ability to work collaboratively on multidisciplinary project teams.
• Strong knowledge of Clinical Drug Development Process, FDA/ICH guidelines, and industry standard data management practices.
• Strong knowledge and experience with EDC systems (Medidata RAVE preferred).
• Proficiency in Microsoft Office.
• Excellent oral and written communication skills.
• Strong project management skills.
• Travel required: 5‑10% (Industry Conferences, Investigator Meetings, Regulatory Inspections as needed).

If you are intrigued by this role but your experience isn’t a perfect match, we encourage you to apply anyway. You could be one step away from a transformative career.

Uniquely Interesting Work, Life‑Changing Careers

Driven by the vision of “Transforming patients’ lives through science,” BMS empowers employees with talent, unique perspectives, and a supportive culture. Our shared values of passion, innovation, urgency, accountability, inclusion, and integrity unlock the highest potential of our teams.

On‑Site Protocol

BMS determines work location based on role requirements: site‑essential, site‑by‑design, field‑based, or remote‑by‑design. Occupancy type is defined by role responsibilities and may include 100% onsite, hybrid, or remote work.

Supporting People with Disabilities

BMS is dedicated to ensuring people with disabilities can excel through transparent recruitment, reasonable accommodations, and ongoing support. For assistance, contact adastaffingsupport@bms.com. Visit our Equal Employment Opportunity statement.

Candidate Rights

BMS considers qualified applicants with arrest and conviction records per applicable laws.

Data Protection

We will never request payments, financial information, or social security numbers. Learn more here. All data processed during the application is protected per applicable privacy policies and regulations.

Seniorities and Employment Types

• Seniority level: Mid‑Senior level
• Employment type: Full‑time
• Job function: Other
• Industries: Pharmaceutical Manufacturing

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