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Senior Director, Clinical Data Management, Therapeutic Area Lead, Melanoma, Hybrid

Merck

RemoteRahway, 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
Hybrid
Level
Staff
Salary
$173.2k – $272.6k/yr
Posted
Aug 13, 2026

Skills

GCPSpark

About this role

Job Description

The Senior Director, Clinical Data Management TA Lead, Melanoma provides strategic and operational oversight of data management delivery across the assigned therapeutic area(s). The role leads portfolio planning, resource and performance management, and cross-functional alignment to ensure execution against GDMS and enterprise priorities. The Senior Director partners with Therapeutic Area (TA), Geography (Geo), and Capability Leads to optimize efficiency, standardization, and digital enablement across programs, while driving quality, compliance, and continuous improvement within the TA organization.

Responsibilities

Accountable for TA (Therapeutic Area) portfolio strategy and prioritization, developing the TA roadmap and study sequencing, and balancing resources, timelines, and risks to meet enterprise commitments. Partner with Clinical Data Manager Geographic Leadership to ensure seamless global delivery, effective knowledge sharing, in depth understanding of protocols, risk-based data management and quality-by-design execution proportionate to study design and therapeutic area risk management across all in-scope data modalities. Partner with Clinical, BARDS (Biostatistics and Research Data Science), GDIA (Global Data Integration & Automation), GCDS (Global Clinical Data Standards), and platform/analytics teams to embed standards, automation, and data-integration practices into TA operating models; define requirements, drive adoption of fit-for-purpose tools, establish TA dashboards and KPIs, and scale successful automation pilots. Forecast capability and capacity needs across regions and programs in partnership with Portfolio and Geographic Leads, optimizing onshore, offshore, and contingent delivery models. Lead TA-wide quality governance, inspection readiness, and risk management; harmonize Corrective And Prevention Action (CAPA) tracking across the portfolio; and present TA performance in reviews with recommended corrective actions and structural improvements. Serve as escalation point for complex study and program issues; capture and scale lessons learned and best practices; and partner with GDMS (Global Data Management & Standards), GCTO (Global Clinical Trial Operations), and GCD (Global Clinical Development) leadership on enterprise-aligned transformation initiatives (including but not limited to process, standards, and platform / tools), ensuring consistent cross-regional adoption and alignment with digital, data, and regulatory guardrails. 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; manage sensitive employee-relations matters in partnership with HR. Balance workloads to support value-added work and work–life sustainability; anticipate obstacles and adjust plans. Coordinate on-shore/off-shore and contingent resources; ensure role clarity and effective handoffs. Manage an operating budget and optimize spend against priorities. Align teams around a clear direction; facilitate team/functional meetings. Provide concise, decision-ready updates and status reporting to leadership and partners. Global Capability Leadership (as assigned) Sit on the CDM (Clinical Data Management) Leadership team as the representative for their assigned capability Contributes to/ leads execution of the strategic objectives and roadmap for capability development initiatives aligned to business needs and industry best practices. Supports governance aligned to GDMS/GCTO policies and enterprise digital / data initiatives. Own development of critical capabilities (tools, processes, skills) aligned to business needs and industry best practices. Establish capability governance aligned with GDMS/GCTO policies and enterprise digital/data initiatives. Drive

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Senior Director, Clinical Data Management, Therapeutic Area Lead, Melanoma, Hybrid at Merck, Rahway, New Jersey, United States of America | Yoinka