Clinical Research Assistant

McLaren Health Care

Mount Pleasant, MIFull-timeNo compensation foundTracked 1w agoSeen in employer's feed 4 days ago

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At a glance

Compensation
No compensation found
Location
Mount Pleasant, MI
Schedule
Full-time
Work Authorization
Not specified

Job overview

McLaren Health Care is hiring a Clinical Research Assistant. Provides support to the clinical research coordinator or clinical research nurse, delivering general administrative assistance, organizing materials, managing data entry, maintaining files and logs, updating the Clinical Trials Management System, obtaining required signatures, and responding to internal and external customer requests while ensuring study compliance with protocol guidelines.

Key focus areas include Provides general administrative assistance including organizational processes, materials management and data entry support, Maintains files, logs and other materials in an organized, efficient manner, and Assists clinical research staff to ensure study requirements are documented and meet regulations.

Skills & qualifications

RequiredNice to have

Qualifications

High School DiplomaSix Months Experience With Data EntryOffice Experience in a Medical Setting

Full job description

Clinical Research Assistant

Michigan, Mount Pleasant (https://careers.mclaren.org/jobs/37363/other-jobs-matching/location-only)

Administrative/Clerical

McLaren Health Care Corp

26004377 Requisition #

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Position Summary:

Provides support to the clinical research coordinator or clinical research nurse.

Essential Functions and 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.

Qualifications:

Required:

  • High school diploma

Preferred:

  • Six months experience with data entry.

  • Office experience in a medical setting.

Additional Information

  • Schedule: Full-time

  • Requisition ID: 26004377

  • Daily Work Times: 8am - 4:30pm

  • Hours Per Pay Period: 80

  • On Call: No

  • Weekends: No

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