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Locum Clinical Trial Manager Jobs (NOW HIRING)

Clinical Trial Manager

Fort Detrick, MD · On-site

$125K - $143K/yr

Description Clinical Trial Manager Venesco LLC is seeking Clinical Trial Managers to provide leadership and operational oversight for FDA-regulated clinical studies, ensuring studies are executed in ...

As a Clinical Trial Manager (CTM), you will be part of the Clinical Operations team reporting to the asset's Clinical Trial or Clinical Program Lead. This position will be responsible for the ...

As a Clinical Trial Manager at ICON, you will manage clinical trial operations activities, supporting your team and stakeholders to deliver high-quality outcomes across our clinical programmes. What ...

Clinical Trial Manager

Fort Detrick, MD · On-site

$125K - $143K/yr

Clinical Trial Manager Venesco LLC is seeking Clinical Trial Managers to provide leadership and operational oversight for FDA-regulated clinical studies, ensuring studies are executed in accordance ...

As a Clinical Trial Manager at ICON, you will manage clinical trial operations activities, supporting your team and stakeholders to deliver high-quality outcomes across our clinical programmes. What ...

Clinical Trial Manager

Marlton, NJ · On-site

$95K - $115K/yr

Clinical Trial Manager Marlton, NJ Hope is Here! Impulse Dynamics (USA), Inc. is a fast-growing medical device company that has pioneered a new form of therapy for heart failure called Cardiac ...

Clinical Trial Manager

Fort Detrick, MD · On-site

$125K - $143K/yr

Clinical Trial Manager Venesco LLC is seeking Clinical Trial Managers to provide leadership and operational oversight for FDA-regulated clinical studies, ensuring studies are executed in accordance ...

Clinical Trial Manager

Watertown, MA · On-site

$125 - $150/hr

Clinical Trial Manager Full Time Management Watertown, MA, US 23 days ago Requisition ID: 1144 Salary Range: $138,566.00 To $153,118.00 Annually About C4 Therapeutics: C4 Therapeutics (C4T) (Nasdaq:

Clinical Operations Team Build | Bay Area | CTA/ CRA, Clinical Trial Manager, and Clinical Program Manager I am running a team build for a clinical-stage medical device company in the Bay Area! Early ...

Clinical Operations Team Build | Bay Area | CTA/ CRA, Clinical Trial Manager, and Clinical Program Manager I am running a team build for a clinical-stage medical device company in the Bay Area! Early ...

Clinical Operations Team Build | Bay Area | CTA/ CRA, Clinical Trial Manager, and Clinical Program Manager I am running a team build for a clinical-stage medical device company in the Bay Area! Early ...

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Locum Clinical Trial Manager information

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How much do locum clinical trial manager jobs pay per hour?

As of Sep 8, 2026, the average hourly pay for locum clinical trial manager in the United States is $62.52, according to ZipRecruiter salary data. Most workers in this role earn between $50.72 and $70.43 per hour, depending on experience, location, and employer.

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Infographic showing various Locum Clinical Trial Manager job openings in the United States as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 85% Physical, 2% Hybrid, and 13% Remote job distribution, with an average salary of $130,034 per year, or $62.5 per hour.

Clinical Trial Manager

VENESCO, LLC

Fort Detrick, MD • On-site

$125K - $143K/yr

Full-time

Re-posted 15 days ago


Job description

Description

Clinical Trial Manager  


Venesco LLC is seeking Clinical Trial Managers to provide leadership and operational oversight for FDA-regulated clinical studies, ensuring studies are executed in accordance with approved protocols, budgets, timelines, regulatory requirements, and quality standards.   

Requirements

Duties and Responsibilities 

  • Manage all phases of clinical trial startup, conduct, and closeout. 
  • Develop and maintain project plans and timelines. 
  • Coordinate protocol development and study documentation. 
  • Manage Trial Master File (TMF) documentation. 
  • Coordinate study working groups and stakeholder meetings. 
  • Ensure ClinicalTrials.gov registration and reporting requirements are met. 
  • Monitor study metrics and status reports. 
  • Coordinate interactions among sites, CROs, sponsors, and regulatory personnel. 
  • Identify operational risks and develop mitigation plans. 
  • Support FDA inspections and sponsor audits. 


Minimum Qualifications 

  • Bachelor's degree in Life Sciences or related field. 
  • Minimum 7 years of clinical trial management experience. 
  • Experience managing FDA-regulated studies. 
  • Strong understanding of ICH-GCP and FDA requirements. 


Venesco, LLC, is an equal opportunity and affirmative action employer. Venesco is committed to administering all employment and personnel actions on the basis of merit and free of discrimination based on race, ethnicity, religious affiliation, gender, gender identity or expression, sexual orientation, national origin, protected veteran status, or status as an individual with a disability. Consistent with this commitment, we are dedicated to the employment and advancement of qualified minorities, women, individuals with disabilities, protected veterans, persons of all ethnic backgrounds and religions according to their abilities.

For more information on Venesco, LLC., visit https://venesco.com.