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Senior Director Clinical Data Management

Merck

Rahway, New Jersey, United States of AmericaFull TimeStaff$173.2k – $272.6k/yr
Sign in to applyVerified 2h ago
Location
Rahway, New Jersey, United States of America
Employment
Full Time
Work model
On-Site
Level
Staff
Salary
$173.2k – $272.6k/yr
Posted
Aug 24, 2026

Skills

GCPSpark

About this role

Job Description

The Senior Director, Data Collection Data Steward (M-track) serves on the GCDS Leadership Team to set strategy and oversee the standards delivery framework, governance, and operations (planning, resourcing, process excellence, and innovation). Drive enterprise metrics and outcomes, act as an escalation point for governance, represent the company externally, and lead people management (objectives, talent, budgets, and communications).

Responsibilities

Provide oversight and guidance to teams as they define and maintain standard data collection (EDC [Electronic Data Capture] and non-EDC modalities) definitions aligned with industry standards (e.g., CDISC [Clinical Data Interchange Standards Consortium]) and Health Authority regulations and guidance Identify opportunities, lead, or participate in organizational initiatives as needed. Support audits and inspections as required. Accountable for the management and timely delivery of standards and governance deliverables, coordinating efforts across GCDS sub-units including resource forecasting, process optimization, operations reviews, and strategic innovation initiatives. Provide oversight and strategic direction to the design and delivery of Standards training and best practices to cross functional teams. Provide oversight and strategic direction to teams in the development of training materials, training delivery, and mentoring of the Global Clinical Data Standards team. Act as a leader in industry forums, maintaining network of contacts, and influence industry strategic direction and clinical data standards development. Build and sustain senior stakeholder networks across GDMS/ Global Clinical Trial Operations (GCTO)/ GCD [Global Clinical Development]) and strategic partners; broker decisions and remove systemic blockers. Provide oversight and expertise within one or multiple TAs on data collection/data transformation design and data modeling to all staff, assuring consistency with established standards guidelines Ability to provide strategic direction and participate in multiple Standards governance initiatives, forums, and reviews (e.g., TAST [Therapeutic Area Standards Team], SLIC [Shared Clinical Data Standards Council]). Lead and/or actively participate in cross-functional (e.g., GDMS/GCTO/GCD [Global Clinical Development]) strategic projects Serve as an escalation point for study-level design, as needed. Provide oversight and strategic direction to teams in development of future standards libraries and/or new/modified processes. Develop the strategic direction for new processes and tools supporting clinical data standards and information management capabilities. Provide oversight and communication of the implementation plans to cross-functional stakeholders and executive management, as appropriate. Provide prioritization and oversight of standards metrics. Communicate metrics cross-functionally to Executive Leadership. Work with fellow GCDS leadership on prioritization and delivery of the Book of Business, new functional programs/projects, and governance demands. Act as an escalation point on governance decisions, including changes to existing library forms and new content. Working in collaboration with GCDS ELT to define the strategic direction and prioritization for the data collection libraries and associated components. Serve as a core member of the GCDS (Global Clinical Data Standards) Leadership Team and proactively engage with stakeholders inside and outside of GCDS and across global sites to drive efforts critical to the success of GCDS and GDMS (Global Data Management and Standards) more broadly. People Management Responsibilities: Set clear objectives aligned to organizational goals; assign work and set priorities. Conduct regular check-ins and annual reviews; coach for performance; provide recognition. Develop career plans; create growth opportunities and promotion cases; ensure appropriate training and mentoring. Lead recruiting and hiring;

Listing verified 2h ago. Applications go through the company's official careers site.

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Senior Director Clinical Data Management at Merck, Rahway, New Jersey, United States of America | Yoinka