Clinical Research Coord I

Job Description

Job Description

Description :

Tanner Clinic has an immediate opening for a Clinical Research Coordinator I.

Essential Job Responsibilities :

• Recruitment and coordination of trial subjects covering informed consent, screening subjects through inclusion and exclusion criteria, and adhering to safety and compliance issues
• Coordination and management of the clinical trial, generating source documents on Microsoft Word, time management, visit coordination, product dispensing and accountability, managing monitoring visits, and communication with sponsor and authorities
• Data collection and management, obtaining medical histories and vital signs, performing phlebotomy, lab processing and shipping, recording and management of AEs, completing CRFs, filing and archiving, and resolving queries
• Other duties as assigned

Requirements : Education :

Experience :

Other Requirements :

Performance Requirements :

Knowledge :

Skills :

Abilities :

Equipment Operated : Standard office equipment including computers, fax machines, copiers, printers, telephones, etc., and medical equipment including ECG machines, blood pressure cuffs, centrifuge, phlebotomy tools, etc.

Work Environment : Position is in a well-lighted office environment. Occasional evening and weekend work.

Mental / Physical Requirements : Involves sitting approximately 50 percent of the day, walking or standing the remainder, but percentage may vary depending on the trials being conducted.