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In-House Clinical Research Associate

Bethesda

Piper Companies Logo

Job Id:
0000174534

Job Category:
Life Sciences

Job Location:
Bethesda

Security Clearance:
No Clearance

Business Unit:
Piper Companies

Division:
Not Defined

Position Owner:
Kamille Purcell

Job Summary:

Piper Companies is seeking an In-House Clinical Research Associate to support a clinical research organization providing clinical trial management and regulatory support services. This position is hybrid in Bethesda, MD, with 2 days onsite and 3 days remote per week.

Responsibilities for the In-House Clinical Research Associate include:

  • Review and process essential regulatory documents received from clinical trial sites.
  • Maintain and organize Trial Master Files (TMF) within electronic document management systems.
  • Track regulatory documents and study records in centralized web-based databases.
  • Evaluate documentation for completeness and compliance with FDA, ICH-GCP, sponsor, and SOP requirements.
  • Coordinate the collection of missing or incomplete site regulatory documentation.
  • Assist with study start-up, monitoring visit preparation, and follow-up activities.
  • Collaborate with CRAs, project managers, site personnel, and sponsors to support ongoing clinical trial operations.

Required Qualifications for the In-House Clinical Research Associate include:

  • Bachelor’s degree in a health-related field or Licensed Practical Nurse (LPN) credential.
  • 2–5 years of experience within a clinical research, pharmaceutical, CRO, sponsor, or clinical site environment.
  • Experience reviewing and collecting regulatory documents in support of clinical trials.
  • Specialized experience with eTMF systems such as Veeva Vault and associated system administration activities.
  • Knowledge of FDA regulations, ICH-GCP guidelines, and clinical research compliance requirements.
  • Strong proficiency with Microsoft Office, including Word, Excel, and Outlook.

Preferred Qualifications for the In-House Clinical Research Associate include:

  • Experience with IRB submissions and OHRP regulations.
  • Previous experience as a CRA, Study Coordinator, IRB Coordinator, or Regulatory Specialist.
  • Experience maintaining Trial Master Files within sponsor or CRO environments.
  • Strong organizational skills with the ability to manage multiple priorities and deadlines.

Compensation for the In-House Clinical Research Associate includes:

  • Salary Range: $50,000–$80,000 annually
  • Full Benefits Package: PTO, Paid Holidays, Medical, Dental, Vision, 401K, Tuition Reimbursement, Paid Maternity Leave, Military Reserve Pay Offset

 

This Job opens for applications on 9/16/2026. Applications for this job will be accepted for at least 30 days from the posting date.

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