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Job description
Direct message the job poster from Medix™
Helping Sponsors take their products from conception ➡ commercialization
We are looking for an experienced CRC to join an exciting and rapidly growing site network in South Minneapolis!
Must have sponsor funded trial experience
Must have trial experience as a CRC from study start up to closeout
Bilingual in Spanish and Phlebotomy experience are HIGHLY preferred
Job Description
Responsibilities will include: Recruiting, screening, and enrolling study patients as well as ensuring patient adherence to study protocol. Dispensing of study drug and drug accountability. Scheduling and conducting patient visits per protocol, including obtaining informed consent. Performing ECGs, collecting blood and urine specimens, taking manual vitals. Processing, packaging and shipping of lab specimens. Issuing and ensuring accuracy of patient diaries. Providing administration of questionnaires. Adverse event reporting. Con med reporting. Managing ancillary study supplies. Timely data entries into electronic data capture (EDC) systems or case report forms (CRFs). Timely resolution of data queries.
Credentials
2+ years of experience as a Clinical Research Coordinator
Seniority level
Associate
Employment type
Full-time
Job function
Science and Research
Industries
Research Services, Pharmaceutical Manufacturing, and Biotechnology Research
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Worksite address
minneapolis, MN, 55400, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.