Coordinator Clinical Research

McLaren Health Care; Flint (MI); On-site; USD 42,000 - 62,000; Full time

Job summary

McLaren Health Care is seeking a Clinical Research Coordinator to facilitate studies, evaluate patient eligibility, assist in informed consent, monitor protocol compliance, and coordinate data collection across site personnel.

The role includes enrolling eligible patients, submitting data to sponsors, coordinating tests, and maintaining regulatory documentation with IRB and sponsor requirements.

Qualifications

• Must have a High School Diploma or equivalent.

Responsibilities

• Evaluates eligibility of candidates for clinical trials by reviewing protocol requirements and data.
• Assists with informed consent and ensures patients have adequate information for consent.

Skills

Informed consent

Data collection

Regulatory compliance

Clinical coordination

Education

High School Diploma or equivalent

Biology/Psychology or related field

SOCRA/ACRP certification

Tools

IRB submission process

Job description

Position Summary

Responsible for facilitating research studies; providing knowledgeable information regarding each research protocol to the medical and nursing staff; evaluating the eligibility of potential candidates for research studies; assisting in the informed consent process; monitoring research study compliance; collecting and submitting data; coordinating required study procedures to meet protocol requirements and maintain a system for effective data flow.

Responsibilities

• Evaluates eligibility of candidates for clinical research studies by reviewing protocol defined eligibility requirements and/or collecting pertinent data on potential candidates, verifying appropriateness of patients for entry to clinical trials, and assisting the other staff in determining eligibility of potential patients.
• Assists the investigator with the informed consent process and assures that the research team and the patient have adequate information to achieve the informed consent process.
• Registers and randomizes eligible patients.
• Submits accurately completed data collection forms to the sponsor or CRO in a timely manner as dictated by the study protocol.
• Coordinates tests and procedures as specified in the study protocol through accurate communication with the site / principal investigator, physicians, patients, nurses, and office/hospital staff.
• Maintains contact with regulatory specialist to ensure data submitted to the IRB of record is accurate and timely. Upon request, submits regulatory documents to regulatory specialist to include in the IRB submission or submission to sponsor or CRO.
• Assists the investigators and clinicians in identifying and enrolling eligible patients into clinical trials/ studies and assures compliance to protocol requirements.
• Educates patients and their families regarding research protocols and keeps them informed of procedures and changes in the studies in which they are participating.

Qualifications

Required

• High School Diploma or equivalent
• Two years’ experience in clinical research or five years in a health care role (e.g., paramedic, emergency medical technician, radiology technician)

Preferred

• Degree in biology, psychology, or other clinical research‑related area or equivalent education and experience
• Three or more years of experience in clinical research
• Clinical research certification through SOCRA or ACRP

Equal Opportunity Employer of Minorities/Females/Disabled/Veterans

Additional Information

• Schedule: Full-time
• Requisition ID: 26002728
• Daily Work Times: 8am - 4:30pm
• Hours Per Pay Period: 80
• On Call: No
• Weekends: No