Bilingual Clinical Research Coordinator
Beacon Hill PharmaRaleigh, NC, US30+ days ago
Job type
- Full-time
Job descriptionRequired : Minimum 2 plus years of hands-on CRC experience at a clinical research site or CRO (will consider Sr. CRC level for more experienced candidates) Experience supporting sponsor-initiated or observational / late-phase clinical trials Comfortable with patient-facing responsibilities including informed consent Ability to independently manage study visits, documentation, and regulatory activities Spanish fluency strongly preferred due to participant demographics Experience with CRIO or another CTMS platform is a plus Clinical / lab skills such as phlebotomy preferred but not required Strong organizational and communication skills; detail-oriented and proactive Be part of a site launch —a rare chance to help build a clinical research hub from the ground up Work in a close-knit, patient-centered environment with national-level operational support Enjoy a clear growth path : CRC and Sr. CRC levels available depending on experience Help expand access to industry-sponsored research in underrepresented communities Opportunity for contract-to-hire conversion with long-term growth potential
Job Description
Job Description
About the Opportunity
We are partnering with a fast-growing, mission-driven research organization dedicated to expanding access to cutting-edge clinical trials in local communities across the U.S. This organization is launching a brand-new clinical site in the RTP area and is seeking a passionate and experienced Clinical Research Coordinator (CRC) to support site startup and active study execution.
Key Responsibilities
- Coordinate and manage daily study activities in compliance with GCP, FDA, and protocol guidelines
- Serve as the primary point of contact for participants, from screening and informed consent through follow-up
- Perform data entry, regulatory documentation, and ensure timely and accurate EDC / CTMS records
- Collaborate with sponsors, CRO monitors, labs, and investigators to ensure clean execution
- Participate in site initiation visits, monitoring visits, and study closeout
- Maintain accurate documentation of study materials, logs, and site files
- Support recruitment, outreach, and compliance tracking
- Oversee inventory and supplies related to protocol requirements
Qualifications
Why You’ll Love This Role
Company Description
A highly reputable compounding pharmacy and FDA-registered outsourcing corporation in Houston, Texas.
Company Description
A highly reputable compounding pharmacy and FDA-registered outsourcing corporation in Houston, Texas.
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Clinical Research Coordinator • Raleigh, NC, US
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