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Overnight Trial Master File Jobs (NOW HIRING)

VENESCO LLC

Clinical Trial Manager

Fort Detrick, MD · On-site

$125K - $143K/yr

Manage Trial Master File (TMF) documentation. * Coordinate study working groups and stakeholder meetings. * Ensure ClinicalTrials.gov registration and reporting requirements are met. * Monitor study ...

VENESCO, LLC

Clinical Trial Manager

Fort Detrick, MD · On-site

$125K - $143K/yr

Manage Trial Master File (TMF) documentation. * Coordinate study working groups and stakeholder meetings. * Ensure ClinicalTrials.gov registration and reporting requirements are met. * Monitor study ...

Character Biosciences

Clinical Trial Manager

Trial Master File: Maintain trial master file completeness and inspection readiness in partnership with study team members * Budget Management: Track study-level spend against budget, flagging ...

Character Bio

Trial Master File: Maintain trial master file completeness and inspection readiness in partnership with study team members * Budget Management: Track study-level spend against budget, flagging ...

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Infographic showing various Overnight Trial Master File job openings in the United States as of September 2026, with employment types broken down into 1% Internship, 1% As Needed, 88% Full Time, 8% Part Time, and 2% Contract. Highlights an 72% Physical, 2% Hybrid, and 26% Remote job distribution, with an average salary of $36,892 per year, or $17.7 per hour.

Clinical Trial Manager

Fort Detrick, MD • On-site

VENESCO LLC
51 - 200 employees
Learn more about VENESCO LLCexternal

$125K - $143K/yr

Full-time

Re-posted 20 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.