Join Our Team as a Clinical Data Manager at Bristol Myers Squibb

Are you ready to embark on a career that is challenging, meaningful, and life-changing? Look no further than Bristol Myers Squibb, where each day presents a unique opportunity to significantly impact patients' lives and grow professionally amidst a diverse and high-achieving team.

About Our Working Environment

At Bristol Myers Squibb, we value the balance and flexibility essential in fostering a productive and happy work environment. We are proud to offer a comprehensive range of benefits and programs aimed at helping our employees achieve their professional and personal goals. Learn more about what makes working with us truly unique at .

Role Overview: Clinical Data Manager

In our pursuit of excellence in clinical data management within the R&D portfolio, we have an exciting opportunity for a Clinical Data Manager. This position plays a crucial role in ensuring the integrity, reliability, completeness, and quality of clinical trial data through robust end-to-end clinical data management.

Key Responsibilities

• Thorough review and management of clinical trial data, ensuring adherence to protocols and data quality standards.
• Efficiently manage data discrepancies and undertake data cleaning tasks to maintain data integrity.
• Collaborate closely with external data vendors and internal teams to assure timely data review and submission.
• Document management responsibilities including accurate filing of documents in the eTMF.

Position Requirements

Educational Background: A Bachelor's Degree in Life Sciences, Pharmacy, or a related field is required.

Experience: At least 2 years of experience in clinical data review or related tasks.

Skill Set: Proficiency in EDC systems (Medidata RAVE preferred), strong Microsoft Office skills, excellent communication abilities, and a foundational understanding of the clinical drug development process and regulations.

Travel: Availability to travel 5-10% for industry conferences, investigator meetings, or regulatory inspections as needed.

Unique Opportunities

If your resume doesn't align perfectly with the job description, we still encourage you to apply. Transforming your career might just be one application away, and we are keen on diversifying clinical trials by aligning unique talents and perspectives with our inclusive culture and shared values.

Worksite Considerations

At Bristol Myers Squibb, your role's nature and responsibilities will determine your worksite classification – from site-essential to remote-by-design positions. Each classification supports our collaborative, innovative, and productive company culture.

Bristol Myers Squibb is committed to creating an inclusive environment for people with disabilities through transparent recruitment processes, reasonable workplace accommodations, and continuous support.

Concerned about health and well-being, Bristol Myers Squibb strongly recommends Covid-19 vaccinations for all employees.

For more information on employment equity and accommodation requests, visit .

Bristol Myers Squibb welcomes all qualified applicants, irrespective of any prior convictions, and processes data in accordance with applicable privacy laws.

Ready to Make a Difference?

Apply today to become a part of a company where you can truly make an impact, not just in your life but in the lives of patients globally. Be a part of transforming patients' lives through science!