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Coordinator Clinical Research

McLaren Health Care Corp -
Flint, MI

Apply Now

Job Details

Full-time

Qualifications

High school diploma or GED

Full Job Description

About Us

McLaren Health Care, headquartered in Grand Blanc, Michigan, is a $7.3 billion, fully integrated health care delivery system committed to quality, evidence-based patient care and cost efficiency. The McLaren system includes 12 hospitals in Michigan, ambulatory surgery centers, imaging centers, a 640-member employed primary and specialty care physician network, commercial and Medicaid HMOs covering more than 732,838 lives in Michigan and Indiana, home health, infusion and hospice providers, pharmacy services, a clinical laboratory network and a wholly owned medical malpractice insurance company. McLaren operates Michigan’s largest network of cancer centers and providers, anchored by the Karmanos Cancer Institute, a National Cancer Institute-designated comprehensive cancer centers. McLaren has 20,000 full-, part-time and contracted employees and more than 113,000 network providers throughout Michigan, Indiana and Ohio.

Coordinator Clinical Research

Michigan, Flint

Health Professional

McLaren Health Care Corp

26002728

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.

Essential Functions and Responsibilities:

1. 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.

2. 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.

3. Registers and randomizes eligible patients.

4. Submits accurately completed data collection forms to the sponsor or CRO in a timely manner as dictated by the study protocol.

5. 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.

6. 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.

7. Assists the investigators and clinicians in identifying and enrolling eligible patients into clinical trials/ studies and assures compliance to protocol requirements.

8. Educates patients and their families regarding research protocols and keeps them informed of procedures and changes in the studies in which they are participating.

#LI-KH1

Qualifications:

Required:

High School Diploma or equivalent
Two years’ experience in clinical research or five-years in a health care role (ex. 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

McLaren Health Care is an Equal Opportunity Employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sexual orientation, gender identification, age, sex, marital status, national origin, disability, genetic information, height or weight, protected veteran or other classification protected by law.

Apply Now

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Coordinator Clinical Research

Michigan, Flint

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