Medix™
Clinical Research Coordinator - 248357
Medix™, San Francisco, California, United States, 94199
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 $20.00/hr - $28.00/hr
Direct message the job poster from Medix™
Part‑Time role (18 hours a week) for 6 months.
Flexible on hours/days worked as long as it is in between the hours of 8am‑5pm Monday‑Friday.
This is a Data entry focused Clinical Research Coordinator role. We are ideally looking for someone with Clinical Research Experience and familiarity with EDC systems.
Position Summary The Clinical Research Coordinator will manage clinical trial activities from study start‑up through close‑out. This role works closely with the research team to collect, manage, and maintain study data in full compliance with FDA regulations, ICH guidelines, and Good Clinical Practice standards.
Responsibilities
Serve as the primary study coordinator—independently or in partnership with a research nurse—responsible for maintaining source documents, collecting and entering data, resolving queries, initiating study payments, coordinating close‑out activities, and communicating with sponsors/CROs.
Collect, verify, and organize clinical data; enter and maintain accurate information in electronic data capture (EDC) systems. Perform data management tasks such as EDC tracking, validation review, updates, SAE and lab reconciliation, and safety coding.
Support regulatory processes as needed, including preparing submissions and maintaining essential regulatory documents in alignment with IRB guidelines.
Seniority level Associate
Employment type Part‑time
Job function Administrative
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Base pay range $20.00/hr - $28.00/hr
Direct message the job poster from Medix™
Part‑Time role (18 hours a week) for 6 months.
Flexible on hours/days worked as long as it is in between the hours of 8am‑5pm Monday‑Friday.
This is a Data entry focused Clinical Research Coordinator role. We are ideally looking for someone with Clinical Research Experience and familiarity with EDC systems.
Position Summary The Clinical Research Coordinator will manage clinical trial activities from study start‑up through close‑out. This role works closely with the research team to collect, manage, and maintain study data in full compliance with FDA regulations, ICH guidelines, and Good Clinical Practice standards.
Responsibilities
Serve as the primary study coordinator—independently or in partnership with a research nurse—responsible for maintaining source documents, collecting and entering data, resolving queries, initiating study payments, coordinating close‑out activities, and communicating with sponsors/CROs.
Collect, verify, and organize clinical data; enter and maintain accurate information in electronic data capture (EDC) systems. Perform data management tasks such as EDC tracking, validation review, updates, SAE and lab reconciliation, and safety coding.
Support regulatory processes as needed, including preparing submissions and maintaining essential regulatory documents in alignment with IRB guidelines.
Seniority level Associate
Employment type Part‑time
Job function Administrative
Referrals increase your chances of interviewing at Medix™ by 2x.
Get notified about new Clinical Research Coordinator jobs in San Francisco, CA.
#J-18808-Ljbffr