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The IMA Group
Overview
Coordinate clinical trials from startup to closeout while serving as the primary contact for participants, sponsors, and CROs. Perform patient-facing procedures including phlebotomy and ensure strict adherence to FDA and ICH-GCP guidelines.
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Compensation
$50,000 - $65,000 / YEAR
Posted
4 days ago
Headlands Research
The CRC manages Phase II-IV clinical studies from initiation to close-out, ensuring compliance with FDA and GCP guidelines. Key duties include conducting subject visits, managing recruitment, and maintaining accurate clinical documentation.
Salary not listed
10 days ago
The Clinical Research Coordinator will manage and execute Phase II-IV clinical studies while ensuring compliance with FDA regulations and GCP/ICH guidelines. Responsibilities include subject recruitment, data entry, documentation, and collaborating with investigators and lab teams to maintain study integrity.
11 days ago
Main Line Health
Manage a variety of cardiovascular device trials and support Phase II-IV drug studies. Coordinate study procedures according to protocols while collaborating with physician investigators and clinical teams.
25 days ago
Coordinate clinical trials according to protocols and SOPs while maintaining accurate ALCOA documentation. Communicate with sponsors, CROs, and IRBs to ensure study data integrity and report adverse events.
$24 - $32 / HOUR
1 month ago
Coordinate clinical trials in accordance with study protocols and standard operating procedures while maintaining accurate documentation. Support investigators, communicate with regulatory bodies and sponsors, and ensure the integrity of study data and adverse event reporting.
$60,000 - $65,000 / YEAR
The Principal Investigator will lead clinical trials, ensuring strict adherence to study protocols and regulatory requirements. They are responsible for evaluating participant eligibility, monitoring patient safety, and maintaining accurate study documentation.
