Clinical Trial Specialist (Hybrid)

Piper Companies is seeking a Clinical Trial Specialist (IRB) to support a well‑established CRO in Bethesda, MD . This hybrid role (2 days on‑site) plays a key part 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 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 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 a science‑related field Compensation Salary: $50,000–$70,000 annually, commensurate with experience Comprehensive benefits: medical, dental, vision (through Cigna), 401k, sick leave required as by law, PTO, holidays #J-18808-Ljbffr