Job Title

We are looking for an experienced CRC to support a site services client of ours.Schedule/Shift: M-F 8a-5p, fully on siteDuration: ~12 monthsMust have experience processing and shipping biological samplesJob DescriptionResponsibilities 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.Credentials2+ years of experience as a Clinical Research Coordinator working on industry sponsored trialsExperience processing, packaging and shipping lab specimens