Clinical Research Coordinator

Barrington James; Town of Florida (NY); On-site; USD 60,000 - 80,000; Full time

Job summary

A leading staffing firm is seeking a Clinical Operations Recruitment Consultant in the Town of Florida, New York. This full-time, on-site contract role supports multiple Alzheimer’s Disease clinical trials. Responsibilities include managing study operations, overseeing clinical research tasks, and leading the site team to ensure enrollment targets. Candidates must have a valid RN license with at least 2 years of experience in related clinical trials. Immediate start available, with strong potential for permanent placement.

Qualifications

• Registered Nurse (RN) license with minimum 2 years' experience as Clinical Research Coordinator (CRC).
• Proven ability to work under pressure and manage several enrolling studies.
• Exhibits calm leadership and communicates effectively with teams.

Responsibilities

• Lead Clinical Research Coordinator overseeing clinical studies.
• Manage study operations and collaborate with CROs/sponsors.
• Perform clinical tasks such as vitals and phlebotomy.

Skills

RN license

Experience on Alzheimer's Disease clinical trials

Strong communication skills

Ability to manage multiple studies

Job description

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