Clinical Research Coordinator: Trials & Compliance Lead

Memorial Healthcare

Owosso (MI)

On-site

USD 52,000 - 68,000

Full time

14 days+

Application generator

Turn this role into an interview — a resume and cover letter built around what this employer wants.

Get past ATS filters

Job summary

Memorial Healthcare in Owosso, MI seeks a Clinical Research Coordinator to support multiple studies under the Principal Investigator. You will ensure compliance with GCP, FDA, IRB, and local policies while guiding staff on protocol requirements and informed consent.

Responsibilities include coordinating study procedures, collecting data, training staff, maintaining regulatory documents, and communicating with sponsors and IRBs.

Qualifications

Bachelor’s degree with clinical experience preferred.
Minimum 2 years of clinical experience or equivalent trial work.
Proficiency with MS Word, Excel, Outlook and EMR systems.
BLS certification preferred.

Responsibilities

Ensure human subject protections during screening, enrollment, and follow-up.
Coordinate research activities and monitor protocol compliance.
Provide patient education and information on study procedures.
Prepare, process, and ship samples as required by protocols.
Maintain regulatory documents and conduct training for staff.

Skills

Clinical research

Attention to detail

Communication

Teamwork

Education

Bachelor’s degree in science/health-related field or business administration

Tools

MS Word

MS Excel

Outlook

EMR systems

IATA knowledge

Job description

Responsibilities include coordinating study procedures, collecting data, training staff, maintaining regulatory documents, and communicating with sponsors and IRBs.

Get your free, confidential resume review.

or drag and drop your file here.