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Senior Clinical Study Manager Jobs (NOW HIRING)

The Senior Clinical Study Manager is responsible for managing clinical trial execution from feasibility assessments through study closeout. This position reports to the Senior Manager Clinical ...

The Senior Clinical Study Manager is responsible for managing clinical trial execution from feasibility assessments through study closeout. This position reports to the Senior Manager Clinical ...

As Senior Clinical Study Manager, you will serve as the cross-functional project leader responsible for delivering clinical research business initiatives through effective project execution ...

As Senior Clinical Study Manager, you will serve as the cross-functional project leader responsible for delivering clinical research business initiatives through effective project execution ...

Clinical Study Manager

Durham, NC ยท On-site

$56.99 - $71.32/hr

Job Title: Clinical Study Manager Location: Durham, NC Pay rate: $56.99 - $71.32/hr. Zip Code: 27701 Area Code: 919 Start Date: Right Away Keywords: #DurhamJobs; #ClinicalStudyJobs; Benefits:

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Senior Clinical Study Manager information

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$22K

$125.3K

$206K

How much do senior clinical study manager jobs pay per year?

As of Sep 5, 2026, the average yearly pay for senior clinical study manager in the United States is $125,290.00, according to ZipRecruiter salary data. Most workers in this role earn between $85,000.00 and $157,000.00 per year, depending on experience, location, and employer.

What does a senior clinical study manager do?

A Senior Clinical Study Manager oversees the planning, execution, and management of clinical trials to ensure they comply with regulatory standards and meet study objectives. They coordinate with cross-functional teams, manage study timelines and budgets, and ensure data integrity. Additionally, they are responsible for monitoring the progress of trials, resolving issues that arise, and communicating results to stakeholders. Their role is critical for advancing medical research and ensuring that new treatments are safe and effective.

How does a senior clinical study manager typically collaborate with cross-functional teams during a study?

A Senior Clinical Study Manager works closely with cross-functional teams such as data management, regulatory affairs, biostatistics, medical writing, and clinical operations to ensure smooth study execution. They facilitate regular meetings, coordinate timelines, and address challenges that arise across teams, ensuring everyone aligns with study objectives and regulatory standards. This role often requires strong communication and leadership skills to manage dependencies, resolve conflicts, and keep projects on track. Effective collaboration is key to maintaining study quality and meeting project milestones.

What are the key skills and qualifications needed to thrive as a senior clinical study manager, and why are they important?

To thrive as a Senior Clinical Study Manager, you need in-depth knowledge of clinical trial processes, regulatory guidelines (such as GCP and ICH), and a relevant life sciences degree, often complemented by several years of clinical research experience. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and certifications like ACRP or SOCRA are typically required. Strong leadership, organizational, and communication skills help manage cross-functional teams and ensure effective collaboration with stakeholders. These skills are essential for delivering high-quality, compliant studies on time and within budget, ultimately supporting successful drug development.
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What cities are hiring for Senior Clinical Study Manager jobs?

Cities with the most Senior Clinical Study Manager job openings:

Who are the top companies hiring for Senior Clinical Study Manager jobs?

The top employers for Senior Clinical Study Manager jobs are:

What states have the most Senior Clinical Study Manager jobs?

States with the most job openings for Senior Clinical Study Manager jobs include:

Infographic showing various Senior Clinical Study Manager job openings in the United States as of August 2026, with employment types broken down into 87% Full Time, 12% Part Time, and 1% Contract. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $125,290 per year, or $60.2 per hour.

Senior Clinical Study Manager (CSM)

System One

Cleveland, OH โ€ข Remote

$60 - $80/hr

Contractor

Medical, Dental, Vision, Life, Retirement

Re-posted 7 days ago


Job description

Job Title: Senior Clinical Study Manager (CSM) Location: 100% Remote Type: Contract - 6 months with desire to go permanent Compensation: $60.00 - $80.00 Work Model: Remote – offsite

Joule is current looking to hire aSenior Clinical Study Manager (CSM) to support clinical programs focused on cell/gene therapy and oncology for one of our clients. This is a remote, 40-hour/week contract (initial ~6 months) with the potential to renew or convert to full-time based on project need, performance, and budget. In this role, you will lead day-to-day study execution by partnering with CROs, sites, and cross-functional stakeholders while ensuring compliance with ICH-GCP and FDA requirements. The ideal candidate brings 8–10 years of clinical operations experience (including 4–5+ years in study management within pharma/biotech) and is comfortable managing timelines, budgets, vendors, and TMF oversight in a fast-paced environment.

Responsibilities

  • Manage and oversee clinical study activities to ensure compliance with GCP, ICH, and FDA regulations
  • Coordinate with CROs, vendors, and site teams to ensure timely progress of clinical trials
  • Prepare and review study documentation, reports, and progress updates
  • Handle budgets, contracts, and invoices related to clinical studies
  • Ensure TMF management and oversight in accordance with regulatory standards
  • Monitor site activities and ensure site management best practices

Requirements

  • University/college degree (BS/BA/MS) or certification in a related health profession from an appropriately accredited institution
  • 8 – 10 years’ experience, including 4 – 5 years of experience in a pharmaceutical setting
  • Previous study management experience with at least 4 – 5 years of relevant experience
  • Experience in Cell/Gene Therapy and Rare diseases; recent Oncology experience is desirable

System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.

System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.

#LI-EL1 Ref: #568-Clinical


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About System One

Sourced by ZipRecruiter

System One helps employers get work done more efficiently and economically without compromising quality. Over our 35+ year history, we've helped connect thousands of talented people with innovative companies. The excitement of a perfect fit motivates us every single day.

Industry

Business consulting services and recruiting and staffing services

Company size

5,001 - 10,000 Employees

Headquarters location

Pittsburgh, PA, US