Position Summary
The Clinical Research Coordinator will support multiple research studies (government, private and pharmaceutical) through the coordination and implementation of clinical trials and protocols involving human subjects.
Responsibilities
- Responsible for screening, enrollment, and treatment of research subjects in compliance with established regulations and guidelines and internal standard operating procedures.
- Assist with eligibility assessment and obtaining written informed consent as appropriate.
- Function as a liaison with sponsoring agencies and external sites.
- Responsible for collection, processing and storage of study samples.
- Assist with regulatory submissions including protocol review and monitoring.
- Assist with short term projects and provides cross coverage to various research team members as needed.
- Ensure regulatory documents and administrative files for each protocol are up-to-date and adhere to sponsor requirements.
- Maintain Study Manager data entry for all assigned studies.
- Perform additional related duties as needed.
Minimum Qualifications
- Bachelor's Degree or equivalent in education and experience, plus three years related experience
- Excellent organizational and communication (written and verbal) skills
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