Join Our Clinical Data Management Team at Bristol Myers Squibb

At Bristol Myers Squibb, every role offers an engaging, stimulating, and consequential experience—far removed from the ordinary. As a part of our innovative team, you will play a crucial role in making transformative impacts on patients' lives and experience unparalleled opportunities for career growth. Learn more about our fulfilling career opportunities .

About the Role: Associate Manager, Clinical Data Management

Bristol Myers Squibb is currently seeking a dynamic and experienced Associate Manager of Clinical Data Management (CDM). This vital role not only ensures the integrity, reliability, completeness, and quality of clinical trial data but also provides comprehensive leadership across various studies within the BMS R&D portfolio.

Position Details

This full-time, pivotal position within the CDM team allows for up to 50% remote work flexibility over two weeks, blending office presence with the convenience of working from home. Reporting directly to the line manager within CDM, the incumbent will be an essential part of transforming clinical data management processes.

Key Responsibilities

• Study Startup: Collaborate on timelines, develop specifications, perform database and edit checks, and coordinate meetings to ensure a robust start to new clinical trials.
• Study Conduct: Oversee post-production activities, liaise with external data vendors, and support data management staff in clean patient group delivery.
• Study Closeout: Assist in the planning and execution of database lock activities and perform post-lock tasks to ensure study completion with integrity.
• Project Management and Documentation: Support project management tasks and maintain appropriate documentation in electronic Trial Master File (eTMF).
• Training and Mentorship: Provide training and mentorship to junior CDM staff, enhancing team competence and performance.

Requirements and Skills

Prospective candidates should hold a Bachelor’s Degree in Life Sciences, Pharmacy, or a relevant field, coupled with at least 4 years of experience in Clinical Data Review tasks. Strong knowledge of the Clinical Drug Development Process, proficiency with Electronic Data Capture (EDC) systems, particularly Medidata RAVE, and robust Microsoft Office skills are essential. Excellent oral and written communication skills are crucial for this role. Some travel (5-10%) may be required for industry conferences, investigator meetings, or regulatory inspections.

Why Join Bristol Myers Squibb?

Bristol Myers Squibb is not only a leader in the pharmaceutical industry but also a staunch advocate of employee wellness and professional development. We offer a diverse range of competitive benefits and flexible work arrangements to support the goals of our staff both professionally and personally.

Our inclusive culture encourages diversity in clinical trials and champions the unique contributions of each colleague through shared values of passion, innovation, urgency, accountability, inclusion, and integrity.

To apply for this transformative career opportunity as an Associate Manager in Clinical Data Management or to explore other opportunities within Bristol Myers Squibb, please visit .

Bristol Myers Squibb is an equal opportunity employer, committed to fostering a diverse and inclusive workplace. We also accommodate individuals with disabilities throughout the recruitment process. Feel free to direct accommodation requests to [email protected] and review our .

We look forward to considering your application and possibly welcoming you to our team, where you can make a significant impact not only in your career but also in the lives of millions around the globe.