Clinical Research Coordinator - 119425 (Fremont) Job at Medix™, Fremont, CA

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  • Medix™
  • Fremont, CA

Job Description

Contract Length: 3-6 months supporting cardiac device study

Must have experience ding blood draws

POSITION SUMMARY:

The Clinical Research Coordinator (CRC) is responsible for the coordination and administration of clinical trials under the direction of the Clinical Research Manager, the Principal Investigator and the Medical Director. The CRC will develop, implement, and coordinate research and administrative procedures for the successful management of clinical trials. The CRC will perform diverse administrative duties requiring analysis, sound judgment, and a high level of knowledge of study specific protocols.

Duties and Responsibilities:

Administratively and clinically manage an average of six to eight clinical trials

Adhere to Research SOP’s

Adhere to Good Clinical Practices and the study protocols

Ensure scientific integrity of data and protect the rights, safety, and well-being of patients

enrolled in clinical trials

Discuss study protocols with patients and verify the informed consent documentation

Provide patient with written communication of their participation (i.e. copy of the signed

informed consent)

Dispense study medication in a professional and accountable manner following protocol

requirements

Perform ECGs and obtain vital signs of patients

Schedule all patient research visits and procedures consistent with protocol

requirements

Job Tags

Contract work, Part time,

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