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Clinical Trial Program Manager Jobs (NOW HIRING)

VENESCO LLC

Clinical Trial Manager

Frederick, 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 ...

VENESCO, LLC

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 ...

Frontier Medicines

Clinical Trial Manager

Boston, MA · On-site

$120K - $150K/yr

... program strategy and cross-functional leadership. This is a hybrid role based in our Boston, MA ... Clinical Trial Manager or Clinical Project Management experience, ideally supporting oncology ...

Kymera Therapeutics

Clinical Trial Manager

Watertown, MA · On-site

$115K - $200K/yr

Responsible for management of vendors to support clinical trial execution * Plan, execute, and lead study-specific meetings (e.g., internal core team meetings, investigator meetings, etc), as needed

Sagimet Biosciences

Clinical Trial Manager

San Mateo, CA · On-site

$90 - $100/hr

Job Type Contract Description The Clinical Trial Manager manages and leads the day-to-day clinical trial activities related to the development and execution of cross-functional and third-party vendor ...

Alpha-9 Oncology

Clinical Trial Manager

Boston, MA

Manage day-to-day relationships with clinical trial vendors, including tracking vendor contracts, budgets, invoices, and payments against contracted scope of work, and escalating issues or variances ...

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

As of Aug 7, 2026, the average hourly pay for clinical trial program 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.

What does a clinical trial program manager do?

A Clinical Trial Program Manager oversees the planning, execution, and completion of clinical trials within an organization. They coordinate cross-functional teams, manage timelines and budgets, ensure compliance with regulatory guidelines, and maintain the quality and integrity of clinical data. Their role is essential for the successful development of new medical treatments, as they bridge communication between stakeholders, monitor progress, and address any issues that arise during trials.

What are some common challenges faced by clinical trial program managers, and how can they be addressed?

Clinical Trial Program Managers often encounter challenges such as managing complex timelines, coordinating multiple stakeholders, and ensuring regulatory compliance across different study sites. These challenges can be addressed by implementing robust project management tools, maintaining clear and consistent communication with cross-functional teams, and staying updated on regulatory requirements. Developing strong organizational skills and fostering collaborative relationships with investigators, sponsors, and regulatory bodies are also key to overcoming obstacles in this role.

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

To thrive as a Clinical Trial Program Manager, you need strong project management skills, a background in life sciences or healthcare, and experience with clinical research regulations such as GCP, often supported by a relevant degree and certifications like PMP or ACRP. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and regulatory submission tools is typically required. Exceptional leadership, communication, and problem-solving abilities help you coordinate teams and manage complex stakeholder relationships. These skills ensure that clinical trials are conducted efficiently, compliantly, and successfully, leading to reliable study outcomes and regulatory approval.
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Clinical Trial Program Manager jobs near you
Infographic showing various Clinical Trial Program Manager job openings in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $130,034 per year, or $62.5 per hour.

Clinical Trial Manager

VENESCO LLC

Frederick, MD • On-site

$125K - $143K/yr

Full-time

Posted 12 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.