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Clinical Research Coordinator

Job in City of Rochester, Rochester, Monroe County, New York, 14602, USA
Listing for: Medix™
Full Time, Contract position
Listed on 2026-01-12
Job specializations:
  • Healthcare
    Clinical Research, Medical Science
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below
Position: Clinical Research Coordinator - 247268
Location: City of Rochester

This range is provided by Medix™. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$30.00/yr - $35.00/yr

Direct message the job poster from Medix™

Clinical Research Recruiter | Life Sciences

Job Title:

Clinical Research Coordinator

Schedule: Monday–Friday, 40 hours per week

Contract Type: 4-month contract with the possibility of full-time hire (not guaranteed)

Position Overview

We are seeking a dedicated and detail-oriented Clinical Research Coordinator (CRC) to support clinical trials at a therapeutically driven clinical research site network. This role involves coordinating and conducting study activities in accordance with study protocols, Good Clinical Practice (GCP), and regulatory requirements. The ideal candidate is patient-focused, organized, and experienced in clinical research operations.

Therapeutic Areas
  • Infectious Disease
  • Central Nervous System (CNS)
  • Cardiovascular
  • Metabolic Disorders
Key Responsibilities
  • Obtain and document informed consent from study participants
  • Coordinate, conduct, and perform all study visit procedures per protocol
  • Ensure accurate and timely collection of clinical data and source documentation
  • Assist with monitoring visits, including preparation and follow-up activities
  • Attend investigator meetings as required
  • Assist with query resolution and communication with sponsors and monitors
  • Provide the highest level of care and excellent customer service to study participants
  • Maintain compliance with study protocols, SOPs, and regulatory guidelines
Qualifications & Experience
  • Previous experience as a Clinical Research Coordinator or in a clinical research setting preferred
  • Knowledge of clinical trial operations and GCP guidelines
  • Phlebotomy and laboratory processing experience preferred
  • Strong organizational, communication, and interpersonal skills
  • Ability to manage multiple tasks and studies in a fast-paced environment
  • Patient-facing experience with a focus on quality care and professionalism
  • On-site position at a clinical research site in Rochester, NY
  • Collaborative, research-focused clinical setting
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