We are looking for a full-time experienced Clinical Research Coordinator to join our team.

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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.

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The successful candidate must have: At least 1 - 2 years of experience as a Clinical Research Coordinator. Knowledge of surgical medications, including Anesthesia medications. Strong organizational skills. Proven track record of reliability. The ability to work and solve problems independently. Training in GCP. Certified Research Coordinator preferred but not required.

For consideration, please email your cover letter and resume.

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Job Type: Full-time

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Required experience:

• Clinical Research Coordinator: 2 years