Clinical Research Coordinator - 248147

Medix™; Minneapolis (MN); On-site; USD 60,000 - 80,000; Full time

Job summary

A leading clinical research company in Minneapolis is seeking an experienced Clinical Research Coordinator to manage patient recruitment and protocol adherence. Candidates should have at least 2 years of clinical research experience and preference will be given to those who are bilingual in Spanish and possess phlebotomy skills. This full-time role offers opportunities in a rapidly growing research network.

Qualifications

• Must have experience in clinical research.

Responsibilities

• Recruiting, screening, and enrolling study patients.
• Ensuring patient adherence to study protocol.
• Dispensing study drug and ensuring accountability.
• Scheduling and conducting patient visits.
• Performing ECGs and collecting specimens.
• Timely data entries into electronic data capture systems.

Skills

Sponsor funded trial experience

Trial experience from study start up to closeout

Bilingual in Spanish

Phlebotomy experience

Education

2+ years of experience as a Clinical Research Coordinator

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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