Overview:
The Clinical Research Assistant I is responsible for the coordination, collection, processing and quality control of clinical trial data under the direct supervision of the Manager Clinical Research. Maintains all research protocol data and compliance reporting. Assists with screening of and consent from patients for research protocol regimens.
Dedicated to excellence in all aspects of clinical research with a keen focus on ethics, safety, quality, compliance and stewardship.
Responsibilities:
* Maintains patient data files and protocol documents in an organized manner for easy retrieval and review. Accurately and efficiently abstracts information from the EHR for multiple protocols.
* Ensures accurate data collection, entry and timely submission to the appropriate sponsors. Identifies data discrepancies and errors and amends or corrects data discrepancies in consultation with the investigator and research team.
* Assists with scheduling consultations, diagnostic tests or procedures, future appointments for patients as requested. Coordinates scheduling for patients for other study protocols as assigned.
* Conduct patient phone calls and patient visits as delegated.
* Works with research coordinators and research nurses in acquiring or uploading or shipping radiology scans, medical procedures, tissue, labs, etc. as needed per each individual protocol.
* Assists in maintaining study supplies, lab kits, and storage facilities for clinical research as needed.
Qualifications:
* Education: High School or GED, required. 4 Year / Bachelors Degree, preferred.
* Experience: Clinical Research or healthcare/medical experience preferred. Associate's degree may substitute for 1 year of experience or Bachelor's degree may substitute for 2 years of experience; Master's degree may substitute for 3 years of experience. Certification (ACRP/SOCRA/equivalent) preferred.
* Licensure/Certification/Registration: Valid driver's license in appropriate state, required.
* Additional Skills Required: Must have exceptional organizational and analytical skills. Attention to detail. Self-motivated and able to work independently. Able to meet multiple deadlines for concurrent projects. Work in a team- oriented setting. Must be proficient in Microsoft Office.
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