Barrington James
Clinical Operations Recruitment Consultant - (Contract)
URGENT CRC HIRE.
Onsite - Full Time Contract - Immediate Start
Role overview This is a full‑time, on‑site CRC position supporting multiple clinical trials, combining clinical nursing responsibilities with lead‑level study coordination and site leadership. The role is initially a 6–12 month contract, with strong potential to convert to a permanent position.
Key responsibilities
Serve as lead CRC for clinical studies, overseeing day‑to‑day conduct of assigned protocols.
Manage study operations, including timely responses to CROs/sponsors and close collaboration with monitors during on‑site visits.
Perform core CRC tasks: vitals, phlebotomy, documentation, and visit procedures in accordance with protocol and GCP.
Administer and/or oversee infusions as an RN, with support from two additional team members, to cover the high volume of trials.
Support and guide the site team, helping to ensure enrollment and visit targets are met across current and upcoming protocols.
Required experience and profile
RN
license with at least
2+ years of experience working on Alzheimer's Disease clinical trials
as a CRC or in a closely related capacity.
Demonstrated ability to thrive under pressure and manage multiple enrolling studies at once.
Calm, steady leadership presence with a collaborative, team‑focused approach.
Strong communication skills with sponsors, CROs, monitors, and internal site staff.
Seniority level
Associate
Employment type
Contract
Job function
Research, Analyst, and Information Technology
Industries
Staffing and Recruiting
#J-18808-Ljbffr
Onsite - Full Time Contract - Immediate Start
Role overview This is a full‑time, on‑site CRC position supporting multiple clinical trials, combining clinical nursing responsibilities with lead‑level study coordination and site leadership. The role is initially a 6–12 month contract, with strong potential to convert to a permanent position.
Key responsibilities
Serve as lead CRC for clinical studies, overseeing day‑to‑day conduct of assigned protocols.
Manage study operations, including timely responses to CROs/sponsors and close collaboration with monitors during on‑site visits.
Perform core CRC tasks: vitals, phlebotomy, documentation, and visit procedures in accordance with protocol and GCP.
Administer and/or oversee infusions as an RN, with support from two additional team members, to cover the high volume of trials.
Support and guide the site team, helping to ensure enrollment and visit targets are met across current and upcoming protocols.
Required experience and profile
RN
license with at least
2+ years of experience working on Alzheimer's Disease clinical trials
as a CRC or in a closely related capacity.
Demonstrated ability to thrive under pressure and manage multiple enrolling studies at once.
Calm, steady leadership presence with a collaborative, team‑focused approach.
Strong communication skills with sponsors, CROs, monitors, and internal site staff.
Seniority level
Associate
Employment type
Contract
Job function
Research, Analyst, and Information Technology
Industries
Staffing and Recruiting
#J-18808-Ljbffr