Clinical Research Coordinator (CRC)

Job Description

Submitting regulatory documents to IRB and Sponsor • Preparing for study initiation • Recruiting subjects • Screening and scheduling subjects • Getting voluntary subject consent • Teaching subjects about protocol expectations for them • Performing study/protocol procedures in a detailed, accurate manner • Maintaining study files • Tracking subjects, avoiding lost-to-follow-up • Documenting an adverse event • Maintaining communication and correspondence (by telephone, email, fax, etc.) with subjects, sponsor, monitor and other site study personnel, including: • Completing case report forms (CRA) for PI review and approval • Maintaining study-specific supplies • Preparing for study closure and archiving.

Salary

-

Industry

Functional Area

Medical,

Role

Permanent Job, Full time

Other Benefits

N/A

Primary Responsibilties

Submitting regulatory documents to IRB and Sponsor • Preparing for study initiation • Recruiting subjects • Screening and scheduling subjects • Getting voluntary subject consent • Teaching subjects about protocol expectations for them • Performing study/protocol procedures in a detailed, accurate manner • Maintaining study files • Tracking subjects, avoiding lost-to-follow-up • Documenting an adverse event • Maintaining communication and correspondence (by telephone, email, fax, etc.) with subje

Required Qualification

UG - Bachelor of Pharmacy (B.Pharma) - Any Specialization

PG - Master of Pharmacy (M.Pharma) - Any Specialization

Cerification - N/A

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