Sr. Clinical Research Coordinator- Endocrinology & Metabolism

About the role

Oversees the day-to-day activities of a clinical trial in accordance with Good Clinical Research Practice (GCP).

Responsibilities

• Runs portions of clinical trials from startup to closeout, including protocol coordination (screening, recruiting, enrolling, consenting), feasibility planning, data management, biological specimen management, preparation for monitoring visits, and regulatory and/or IRB document preparation.
• Ensures all study procedures are conducted according to the protocol and applicable regulations.
• May assist with the orientation and training of new staff.
• Assists in the development of workflows, training documents, SOP/guidance document revision.
• Participates in work groups.

Requirements

• Minimum High School Diploma or equivalent.
• AND
• High School Diploma or equivalent and SoCRA certification and 6 years of clinical research experience OR Bachelor’s degree and 2 years of clinical research experience OR Master’s Degree and 1 year clinical research experience.

Qualifications

Education: Minimum High School Diploma or equivalent. AND Experience: High School Diploma or equivalent and SoCRA certification and 6 years of clinical research experience or Bachelor’s degree and 2 years of clinical research experience or Master’s Degree and 1 year clinical research experience.

Skills

N/A

Benefits

N/A

Pay

N/A

Schedule

N/A