Clinical Research Coordinator: Drive Trial Operations

mclarenhlth; Flint (MI); On-site; USD 52,000 - 76,000; Full time

Job summary

McLaren Health in Flint, MI is seeking a Clinical Research Coordinator to facilitate studies, evaluate eligibility, and coordinate protocol procedures with medical teams. The role includes assisting in informed consent, enrolling patients, and ensuring timely data submission to sponsors.

Preferred qualifications include a biology or related degree and SOCRA/ACRP certification, with 3+ years in clinical research highly valued. Equal opportunity employer.

Qualifications

• High School Diploma or equivalent.
• Two years’ experience in clinical research or five years in a health care role.
• Degree in biology, psychology, or related area preferred.
• Three or more years of experience in clinical research preferred.
• Clinical research certification through SOCRA or ACRP preferred.

Responsibilities

• Evaluate eligibility of candidates for clinical studies per protocol requirements.
• Assist investigator with informed consent ensuring adequate information.
• Register and randomize eligible patients.
• Submit completed data forms to sponsor or CRO as dictated by protocol.
• Coordinate tests and procedures per protocol with staff and physicians.
• Maintain regulatory submissions to IRB and regulatory specialists.
• Educate patients and families about protocols and changes in studies.

Education

High School Diploma or equivalent

Degree in biology or related field

Clinical research certification SOCRA/ACRP

Job description

McLaren Health in Flint, MI is seeking a Clinical Research Coordinator to facilitate studies, evaluate eligibility, and coordinate protocol procedures with medical teams. The role includes assisting in informed consent, enrolling patients, and ensuring timely data submission to sponsors.

Preferred qualifications include a biology or related degree and SOCRA/ACRP certification, with 3+ years in clinical research highly valued. Equal opportunity employer.