Associate Director Study Manager (Hybrid)
M
Merck
📍 North Wales, PA, United States
Job Description
**Job Description**
**Role Overview:** The Associate Director Study Manager leads the operational planning, execution, and delivery of one or more global clinical trials. This role is accountable for ensuring high-quality study conduct, driving timelines, managing risks, and coordinating across internal and external stakeholders to meet clinical trial objectives.
**Key Responsibilities:**
+ Lead operational planning, feasibility assessment, and execution of assigned clinical trials(s)
+ Serve as the Clinical Trial Team (CTT) Lead and provide cross-functional leadership
+ Drive study strategy, operational reviews, and risk identification and mitigation planning
+ Collaborate with internal teams, country organizations, and external partners (e.g. CROs, vendors) to deliver study objectives
+ Oversee study timelines, key deliverables, and execution milestones
+ Provide operational input into clinical trial documents (protocols, plans, reports)
...
**Role Overview:** The Associate Director Study Manager leads the operational planning, execution, and delivery of one or more global clinical trials. This role is accountable for ensuring high-quality study conduct, driving timelines, managing risks, and coordinating across internal and external stakeholders to meet clinical trial objectives.
**Key Responsibilities:**
+ Lead operational planning, feasibility assessment, and execution of assigned clinical trials(s)
+ Serve as the Clinical Trial Team (CTT) Lead and provide cross-functional leadership
+ Drive study strategy, operational reviews, and risk identification and mitigation planning
+ Collaborate with internal teams, country organizations, and external partners (e.g. CROs, vendors) to deliver study objectives
+ Oversee study timelines, key deliverables, and execution milestones
+ Provide operational input into clinical trial documents (protocols, plans, reports)
...