Medix™
Base pay range
$33.00/hr - $37.00/hr
About this role Looking for a strong Clinical Research Coordinator to join our team!
Start Date:
December 1st Location:
100% onsite
Responsibilities
This is a 6 month contract to hire (based off performance/attendance)
Must have Clinical Research Coordinator experience
Experience with weight loss, diabetes or endocrinology studies
Coordinate and manage all aspects of assigned Phase 2–4 clinical trials from site initiation to close‑out.
Conduct study visits, including obtaining informed consent, performing protocol‑required procedures, and collecting source data using eSource systems.
Ensure timely and accurate entry of study data into electronic case report forms (eCRFs).
Utilize eSource, eConsent, eISF, and other clinical trial software platforms to maintain complete, accurate, and regulatory‑compliant study records.
Support site readiness and compliance with 21 CFR Part 11, ICH GCP, and sponsor SOPs.
Maintain up‑to‑date regulatory documents and study binders (electronic and/or paper as required).
Assist with preparation for sponsor, CRO, or regulatory audits.
Recruit, screen, and enroll study participants according to protocol inclusion/exclusion criteria.
Ensure ongoing patient safety by monitoring for adverse events and reporting per protocol.
Serve as the primary point of contact for sponsors, CROs, monitors, and other site staff.
Provide on‑site support at additional study locations when required (occasional travel).
Support training and mentoring of new CRC staff as assigned. Seniority level Associate
Employment type Full‑time
Job function Research
Industries Hospitals and Health Care
Benefits
Medical insurance
Vision insurance
401(k)
#J-18808-Ljbffr
About this role Looking for a strong Clinical Research Coordinator to join our team!
Start Date:
December 1st Location:
100% onsite
Responsibilities
This is a 6 month contract to hire (based off performance/attendance)
Must have Clinical Research Coordinator experience
Experience with weight loss, diabetes or endocrinology studies
Coordinate and manage all aspects of assigned Phase 2–4 clinical trials from site initiation to close‑out.
Conduct study visits, including obtaining informed consent, performing protocol‑required procedures, and collecting source data using eSource systems.
Ensure timely and accurate entry of study data into electronic case report forms (eCRFs).
Utilize eSource, eConsent, eISF, and other clinical trial software platforms to maintain complete, accurate, and regulatory‑compliant study records.
Support site readiness and compliance with 21 CFR Part 11, ICH GCP, and sponsor SOPs.
Maintain up‑to‑date regulatory documents and study binders (electronic and/or paper as required).
Assist with preparation for sponsor, CRO, or regulatory audits.
Recruit, screen, and enroll study participants according to protocol inclusion/exclusion criteria.
Ensure ongoing patient safety by monitoring for adverse events and reporting per protocol.
Serve as the primary point of contact for sponsors, CROs, monitors, and other site staff.
Provide on‑site support at additional study locations when required (occasional travel).
Support training and mentoring of new CRC staff as assigned. Seniority level Associate
Employment type Full‑time
Job function Research
Industries Hospitals and Health Care
Benefits
Medical insurance
Vision insurance
401(k)
#J-18808-Ljbffr