Clinical Trial Specialist (Hybrid)

Piper Companies is seeking a Clinical Trial Specialist (IRB) to support a well-established CRO in Bethesda, MD. This role is hybrid (2 days on-site) and will play a key role in supporting clinical trial operations by ensuring the TMF is accurate, compliant and audit-ready.

• This is a short-term assignment of 3+ months Responsibilities of the

Clinical Trial Specialist:

• Maintain, organize, and track all regulatory documents (IRB submissions, renewals, amendments, CRF, ICF, etc..)
• Perform routine quality checks and provide TMF metrics and status reports to internal teams and sponsors
• Ensure timely filing, retrieval, and delivery of clinical trial documents
• Support audit and inspection readiness activities
• Contribute to updates of SOPs, work instructions, and training materials related to TMF processes Qualifications of the

Clinical Trial Specialist:

• 1-3+ years of regulatory submission/IRB experience working for a CRO, pharmaceutical/biotech, or research institution
• Must have prior IRB submission/regulatory experience
• Strong database experience in Veeva Vault, eTMF, RedCap, Medidata, eCRF, etc.
• Bachelor's degree in science related field Compensation for the

Clinical Trial Specialist:

Salary:

$50,000 - $62,000 annually, commensurate with experience

Comprehensive Benefits:

Medical, Dental, Vision (through Cigna), 401k, Sick leave required as by law, PTO, Holidays This job opens for applications on 4/17/2026. Applications for this job will be accepted for at least 30 days from the posting date.

Keywords:

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