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Clinical Trial Program Manager Jobs in Virginia (NOW HIRING)

Clinical Trial Psych Rater

Fairfax, VA ยท Remote

$62K - $156K/yr

Clinical Trial Psych Rater - US Spanish Speaking Location: Remote/Virtual Hours: Estimated 10-16 ... Excellent organizational skills, attention to detail, time management, and problem-solving ability.

... trial program, protocol and patient treatment principles for the trial ensuring a trusted ... Responsible for activities as assigned by manager. * Responsible for continuous risk-assessment ...

... trial program, protocol and patient treatment principles for the trial ensuring a trusted ... Responsible for activities as assigned by manager. * Responsible for continuous risk-assessment ...

... trial program, protocol and patient treatment principles for the trial ensuring a trusted ... Responsible for activities as assigned by manager. * Responsible for continuous risk-assessment ...

$502K - $650K/yr

Successful development and expansion of oncology clinical trial programs. * Increased physician ... Strong relationship management across departments and institutions. Riverside Cancer Care Network ...

We have a very active clinical trial program, pharmaceutical studies, and emerging statewide ... Health System is comprised of eleven member hospitals and five hospitals under management ...

$68K - $93K/yr

Gathers and records all required study related to the Clinical Trial Management System (CTMS). Reports all Serious Adverse Events (SAE) to the Principle Investigator, monitor, sponsor, and IRB as ...

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Clinical Trial Program Manager information

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.

What cities in Virginia are hiring for Clinical Trial Program Manager jobs?

Cities in Virginia with the most Clinical Trial Program Manager job openings:

Infographic showing various Clinical Trial Program Manager job openings in Virginia as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution.

Clinical Trial & Pharmacovigilance Manager

VENESCO LLC

Falls Church, VA โ€ข On-site

Full-time

Re-posted 10 days ago


Job description

Description:

Clinical Trial & Pharmacovigilance Manager

Location: Hybrid
Job Type: Full-Time

Position Overview:
Venesco is seeking an experienced Clinical Trial & Pharmacovigilance Manager to oversee clinical trial operations and ensure robust safety surveillance practices.


Requirements:

Key Responsibilities: • Manage clinical trial operations from startup through closeout • Oversee adverse event reporting and pharmacovigilance systems • Ensure compliance with ICH-GCP and regulatory requirements • Coordinate DSMB activities and safety reviews • Develop and maintain clinical study documentation • Collaborate with regulatory teams on submissions

Minimum Qualifications: • Advanced degree in clinical research, life sciences, or related healthcare field • 8+ years of clinical operations and safety experience • Strong knowledge of ICH-GCP and FDA regulations

Preferred Qualifications: • Experience with Argus or ArisG safety databases • Clinical trial management certification MUST BE A US CITIZEN and US Board certified MD