Job Description

We are looking to add a Clinical Research Professional to a growing study team. The ideal candidate will feel comfortable in a research environment with minimal oversight and exemplify strong understanding of the full trial process. This is full time onsite M-F, competitive salary and benefits. Sponsorship is not available for this role at this time.

Duties

• Manage 1–3 patient visits per day, with periodic admin-focused days as new studies launch.
• Perform certified phlebotomy/blood draws and operate centrifuges.
• Partner with onsite clinic techs and embedded clinic staff to ensure smooth study flow.
• Input clinical trial data across various study-specific EDC platforms in a timely manner.
• Maintain standard regulatory binders and study documentation.
• Oversee IP processes (without direct drug dispensing) and host/meet with external study monitors.

Required Skills & Qualifications

• Certified for phlebotomy / blood draws.
• Hands-on experience operating a centrifuge for specimen processing.
• Proficiency in data entry across various Electronic Data Capture (EDC) platforms.
• Standard clinical research regulatory maintenance and audit readiness.
• Understanding of IP accountability and monitoring processes.
• Proven ability to work independently ("plug-and-play") without direct daily onsite supervision.
• Strong interpersonal skills to interface smoothly with clinic staff, principal investigators, study monitors, and patients.

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