Clinical Trial Support Specialist

McLaren Health Care; Mount Pleasant (MI); On-site; USD 32,000 - 46,000; Full time

Job summary

McLaren Health Care in Michigan is seeking an Administrative Support professional to assist the clinical research coordinator or clinical research nurse. This role focuses on keeping study operations organized and compliant, while providing essential data entry and office support.

You will work on-site with standard hours 8:00 am to 4:30 pm, supporting sponsor visits, CTMS updates, and timely document routing.

Qualifications

• High school diploma required.
• Six months experience with data entry preferred.
• Office experience in a medical setting preferred.

Responsibilities

• Provides general administrative assistance, including but not limited to organizational processes, materials management and data entry support.
• Maintains files, logs and other materials in an organized, efficient manner.
• Assists clinical research staff to assure all study requirements are documented and meet both internal and external regulations in accordance with protocol guidelines.
• Updates the Clinical Trials Management System (CTMS).
• Responsible for obtaining required signatures on clinical trial documents and returning within specified time frames.
• Candidate will receive additional supportive mentoring for skills development after initial orientation.
• Assignments will be determined by supervisor based on skills, training and competence levels.
• Assignments may broaden in complexity with experience requiring increasing self-directed activity.
• Responds to internal and external customer requests in a timely fashion.
• Assists with the coordination of sponsor visits.
• Performs data quality checks as needed.
• Performs other related duties as required and directed.

Skills

Data entry

Education

High School Diploma

Job description

McLaren Health Care in Michigan is seeking an Administrative Support professional to assist the clinical research coordinator or clinical research nurse. This role focuses on keeping study operations organized and compliant, while providing essential data entry and office support.

You will work on-site with standard hours 8:00 am to 4:30 pm, supporting sponsor visits, CTMS updates, and timely document routing.