Clinical Research Coordinator - 256271

Medix™; California (MO); On-site; USD 42,000 - 62,000; Full time

Job summary

Medix is seeking an experienced Clinical Research Coordinator to support a growing MSO client on a fully on-site basis. The role runs Monday through Friday, 8am–5pm, with responsibilities including patient recruitment, screening, enrollment, and adherence to study protocol.

Responsibilities include dispensing study drug, ECGs, specimen collection, questionnaires, adverse event reporting, data entry into EDC/CRFs, and ensuring data queries are resolved in a timely manner.

Qualifications

• 2+ years as a CRC on industry sponsored trials.
• Experience processing, packaging and shipping lab specimens.

Responsibilities

• Recruit, screen and enroll study patients per protocol.
• Dispense study drug and maintain drug accountability.
• Schedule and conduct patient visits, obtain informed consent.
• Perform ECGs, collect blood/urine samples, take vitals.
• Enter data into EDC/CRFs and resolve data queries.

Skills

Clinical Trials

Data Entry

Patient Recruitment

Informed Consent

Tools

EDC systems

Job description

We are looking for an experienced CRC to support a growing MSO client of ours.

Schedule/Shift: M-F 8a-5p, fully on site

Must have experience as a CRC working on industry sponsored clinical trials

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 working on industry sponsored trials
• Experience processing, packaging and shipping lab specimens