Clinical Research Coordinator I

Job Summary: Provide study coordinator/data management/regulatory specialist support to the Clinical Trials Office (CTO).

Responsibilities:

• Assure all study requirements are documented and meet both internal and external regulations in accordance with protocol guidelines.

• Maintain logs, including tracker submissions and update the CTO Oncore database in a timely manner according to CTO SOPs.

• Respond to queries in a timely fashion.

• Schedule and participate in monitoring visits and participate in multidisciplinary team program meetings as required.

• Assist multidisciplinary team in research activities.

Qualifications:

• Bachelor's degree required or equivalent combination of education and experience.

• Medical and/or science experience/education preferred.

• Proficient with the Microsoft suite including Excel and Power point.

• Demonstrated attention to detail.

Equal Opportunity Employer of Minorities/Females/Disabled/Veterans

Additional Information

• Schedule: Full-time

• Requisition ID: 23006279

• Daily Work Times: 8:30am-5pm

• Hours Per Pay Period: 80

• On Call: No

• Weekends: No

Equal Opportunity Employer

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.