Study Manager, Clinical Operations

MSD

Study Manager contributing to clinical trial operations for a leading healthcare company. Developing skills in project management and collaboration across global teams.

Posted 7/29/2026full-timeNorth Wales • California, New Jersey, Pennsylvania • 🇺🇸 United StatesJuniorMid-Level💰 $96,200 - $151,400 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in project management and operational planning for clinical trials, with a strong understanding of regulatory requirements and the ability to effectively communicate and collaborate with diverse stakeholders.

Highest-signal resume keywords

Project ManagementClinical Trial OperationsRegulatory Compliance (GCP, ICH)Communication SkillsTime Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Drug DevelopmentOperational PlanningLab Specimen TrackingStatus Update ReportingProject Planning PrinciplesAnalytical Skills

Soft Skills

Problem SolvingPrioritizationConflict ResolutionCritical Thinking

Tools & Technologies

Microsoft OfficeExcelPowerPointWordOutlook

Industry Keywords

PharmaceuticalClinical ResearchLife Sciences

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Contributes to the operational planning and execution of one or more clinical trials
Develop leadership and technical skills as part of a global, cross-functional team
Apply project management, communication, and collaboration skills in support of clinical trials
Responsible for operational deliverables such as clinical & ancillary supplies planning, lab specimen tracking, status update reports, study close-out activities
Track study timelines using project management tools
Interact with internal and external stakeholders (e.g. study team, vendors, committees) in support of clinical trial objectives

Requirements

What you’ll need

Bachelor’s Degree +2 years of pharmaceutical, clinical drug development, project management, and/or medical field experience -OR- Master’s Degree +1 year of pharmaceutical, clinical drug development, project management, and/or medical field experience
Degree in life sciences, preferred
Working knowledge of clinical research regulatory requirements (e.g. GCP and ICH)
Ability to manage multiple competing priorities with good planning, time management and prioritization skills
Good understanding of the principles of project planning & project management
Building analytical skills to drive operational milestones
Problem solving, prioritization, conflict resolution, and critical thinking skills
Solid communication, writing and presentation skills
Intermediate knowledge in Microsoft office or similar (Excel, PowerPoint, Word, Outlook, etc.)

Benefits

Comp & perks

medical, dental, vision healthcare and other insurance benefits (for employee and family)
retirement benefits, including 401(k)
paid holidays
vacation
compassionate and sick days