Senior Manager, Clinical Data Management

Senior Manager, Clinical Data Management

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Working with Us

Challenging. Meaningful. Life-changing. Those aren't words that are typically associated with a job, but working at Bristol Myers Squibb is far from ordinary. Every day, uniquely interesting work happens in every department—from optimizing a production line to the latest breakthroughs in cell therapy—transforming the lives of patients and the careers of those who do it. You’ll have the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams.

Functional Area Description

Clinical Data Management focuses on ensuring data quality, integrity, & completeness of all data types (eCRF and non‑eCRF) collected in BMS clinical trials from study start to database lock.

Position Summary еще под

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

Position Responsibilities

Responsibilities will include, but are not limited to:

Project Management and Leadership

• Provides clinical data management leadership within the study team to align on and bel 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 closely collaborates 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 documentsátuensire quality and standardization.
• Chairs Data Quality Review meetings with cross‑functional study team members to ensure ongoing review of trial data currency, quality, and completeness.
• Represents DM on cross‑functional project teams & submission teams.
• Leads or supports 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 monitor DM deliverables according to the Service Level Agreement (SLA).

Continuous Improvement Initiatives

• Provides 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.