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VENESCO, LLC

Clinical Research Associate

Fort Detrick, MD · On-site

$100K - $110K/yr

Description Clinical Research Associate Venesco LLC is seeking a Clinical Research Associate (CRA ... Bachelor's degree in Life Sciences, Nursing, Public Health, or related discipline. * Minimum 3 ...

Venesco LLC

Clinical Research Associate

Fort Detrick, MD · On-site

$95K - $105K/yr

Clinical Research Associate Venesco LLC is seeking a Clinical Research Associate (CRA) to provide ... Bachelor's degree in Life Sciences, Nursing, Public Health, or related discipline. * Minimum 3 ...

ClinChoice

Senior Clinical Research Associate

Nursing degree or relevant degree or background preferred. In some cases, an equivalency ... Clinical Research Associate, CRA, Freelance, Permanent, CRO, Contract Research Organization ...

ClinChoice

Senior Clinical Research Associate

Nursing degree or relevant degree or background preferred. In some cases, an equivalency ... Clinical Research Associate, CRA, Freelance, Permanent, CRO, Contract Research Organization ...

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Infographic showing various Research Associate Nurse job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 69% Full Time, 28% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $67,685 per year, or $32.5 per hour.

Clinical Research Associate

Fort Detrick, MD • On-site

VENESCO, LLC
51 - 200 employees
Learn more about VENESCO, LLCexternal

$100K - $110K/yr

Full-time

Re-posted 20 days ago

Job description

Description

Clinical Research Associate


Venesco LLC is seeking a Clinical Research Associate (CRA) to provide clinical monitoring and oversight support to ensure studies are conducted in compliance with protocols, Good Clinical Practice (GCP), FDA regulations, ICH guidelines, and sponsor requirements.


Requirements

Duties and Responsibilities

  • Conduct site qualification, initiation, monitoring, and closeout visits.
  • Perform source data verification (SDV).
  • Review informed consent documentation and study records.
  • Evaluate protocol compliance and identify deviations.
  • Review regulatory binders and essential documents.
  • Generate clinical monitoring reports and follow-up letters.
  • Support site training and communication activities.
  • Track and assist with CAPA implementation.
  • Support audit and inspection readiness.
  • Maintain study documentation and monitoring files.

Minimum Qualifications

  • Bachelor's degree in Life Sciences, Nursing, Public Health, or related discipline.
  • Minimum 3 years of clinical monitoring experience.
  • Knowledge of FDA regulations, ICH-GCP, and clinical research practices.
  • Strong written and verbal communication skills.
  • Ability to travel CONUS and OCONUS.


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.

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