In-House Clinical Research Associate

Job Summary

Piper Companies is seeking an In-House Clinical Research Associate to support a clinical research organization in Bethesda, MD.

Responsibilities

• 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.
• Collaborate with CRAs, project managers, site personnel, and sponsors to support ongoing clinical trial operations.

Requirements

• 3–5 years of experience within a clinical research, pharmaceutical, CRO, sponsor, or clinical site environment.
• Bachelor’s degree in a health-related field or Licensed Practical Nurse (LPN) credential.
• 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

• 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

Salary Range: $50,000–$80,000 annually *depending on experience*

Full Benefits Package: PTO, Paid Holidays, Medical, Dental, Vision, 401K, Tuition Reimbursement, Paid Maternity Leave, Military Reserve Pay Offset

Contact Information

This Job opens for applications on 7/14/2026. Applications for this job will be accepted for at least 30 days from the posting date.

Keywords

In-House Clinical Research Associate, Clinical Research Associate, CRA, Clinical Trials, TMF, Trial Master File, eTMF, Veeva Vault, Regulatory Documents, Clinical Operations, FDA Regulations, ICH-GCP, GCP Compliance, IRB Submissions, OHRP Regulations, Clinical Research Organization, CRO, Study Coordinator, Regulatory Coordinator, Regulatory Specialist, Pharmaceutical Research, Healthcare Industry, Clinical Documentation, Microsoft Office, Contract-to-Hire, Clinical Study Support, Sponsor Studies, Site Management, Regulatory Compliance