Senior Manager, Clinical Data Management

Senior Manager, Clinical Data Management

Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services, and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives.

Functional Area Description

Clinical Data Management key focus is to ensure data quality, integrity, and completeness of all data types (eCRF and non-eCRF) collected in BMS clinical trials from study start to database lock.

Position Summary

The Senior Manager, Clinical Data Management is a leadership role considered essential to the sustainability and success of the BMS R&D pipeline. This role may report into Director, Clinical Data Management or Associate Director, Clinical Data Management. This is an office-based position in BMS New Jersey locations.

Position Responsibilities

Responsibilities will include, but are not limited to :

• Provides clinical data management leadership within the study team to align on and drive data collection requirements for one or more complex clinical development projects.
• Efficiently plans, coordinates, and delivers complete, high quality and reliable clinical trial data in a timely manner for assigned projects.
• Responsible for end-to-end clinical data management activities and serves as a primary point of contact for internal and external study team members.
• Provides strong quality and project oversight over third party vendor responsible for data management deliverables.
• Takes a leadership role to gather content and integration requirements for EDC and close collaboration with partners supporting other data collection systems (eCOA, External Data, Safety Gateway). Enforces data standard conventions and quality expectations for clinical data per defined processes.
• Authors, reviews / revises DM related study plans including Data Quality Management Plan, Data Validation Plans, Data Review Plan, eCRF Completion Guidelines and other study documents to ensure quality and standardization.
• Chairs Data Quality Review meetings with cross-functional study team members to ensure on-going review of trial data currency, quality and completeness.
• Represents DM on cross-functional project teams & submission teams.
• Lead or support the Health Authority inspections and audits.
• Provides coaching and quality oversight of junior Data Management Leads.

FSP / CRO / Vendor Oversight

May act as core member of the study team and provides FSP / CRO / Vendor oversight for end-to-end Data Management activities, manages data currency throughout the trial, and overall monitoring DM deliverables according to the Service Level Agreement (SLA).

Continuous Improvement Initiatives

Provides the relevant support and input to continuous improvement activities within clinical data management. Provides support for CAPA implementation as required.

Degree / Experience Requirements

Bachelor's Degree required with an advanced degree preferred. At least 5 years of relevant industry experience. Project management certification (e.g. PMP) is desirable.

Key Competency Requirements

Able to work collaboratively on multi-disciplinary project teams and develop productive relationships with external vendors. Sound knowledge of Clinical Drug Development Process, FDA / ICH guidelines and industry standard practices regarding data management. Strong knowledge and experience of EDC systems (Medidata RAVE preferred); demonstrated knowledge of Microsoft Office skills and well versed in industry trends and emerging technologies supporting data collection. Strong project management; exhibits expertise in metrics analysis and reporting methodologies. Excellent oral and written communication skills. Communicate effectively with senior management and cross-functional teams. Knowledge of submission requirements, e.g., New Drug Application (NDA) / Biologics License Application (BLA) / Market Authorization Application (MAA).

Travel Required

5-10% Industry Conferences, Investigator Meetings, Regulatory Inspections (as needed).

If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

Compensation Overview

Madison - Giralda - NJ - US : $143,590 - $173,998 Princeton - NJ - US : $143,590 - $173,998 The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee's work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit https : / / careers.bms.com / life-at-bms / . Benefit offerings are subject to the terms and conditions of the applicable plans then in effect.

BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters. BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

Company : Bristol-Myers Squibb Req Number : R1595778 Updated : 2025-10-28 05 : 10 : 11.124 UTC Location : Madison-NJ Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.