Interested candidates are invited to submit a resume/CV and cover letter outlining their qualifications and interest in the position. Applications will be reviewed on a rolling basis until the position is filled. Up to 3 professional references should be made available upon request.
This is the entry level position on the Michigan Medicine CRC Career Ladder. This position provides administrative and coordination support for multiple projects in the conduct of clinical research projects. This position may assist with study coordination but will not be assigned clinical trials independently. This position may provide coordination for clinical research projects such as registries, retrospective data reviews, studies in long-term follow-up, and other non-interventional studies.
We are seeking a highly motivated Clinical Research Coordinator Assistant to join our team. This person will be responsible for providing study support for clinical trials in the Division of Pain Research. This is a fast-paced clinical environment with a dynamic team. Emphasis is placed on maintaining a positive work environment, fostering comradery and encouraging professional development.
Our mission is to improve the quality of life of people with pain. Achieving personalized pain management will transform care, while dedication to our guiding principles enriches the lives of our team members and those in the community.
Knowledge of all 8 competency domains is expected:
- Scientific Concepts and Research Design
- Ethical Participant Safety Considerations
- Investigational Products Development and Regulation
- Clinical Study Operations (GCPs)
- Study and Site Management
- Data Management and Informatics
- Leadership and Professionalism
- Communication and Teamwork
20% Clinical Coordinator Responsibilities (ex. Assist with screening participants for study eligibility & enroll with accuracy in various databases; May complete simple study reimbursement with partners; May provide lab results, not interpretation, to participants)
Demonstrates ability to screen participants for study eligibility & enroll with accuracy in various databases.
Performs simple study procedures with accuracy.
Understands protocol structure and how to interpret study requirements to ensure study compliance.
Understands proper documentation techniques as outlined in the ICH-GCP guidelines.
May complete simple study reimbursement with partners such as the Human Subjects Incentive Program (HSIP) and the CTSU finance team.
Demonstrates the ability to find and utilize information from EMR and databases/CTMS/EDC.
May mark visits as planned/occurred in OnCore.
May provide lab results, not interpretation, to participants.
May maintain essential regulatory documents.
May assist research coordinator in conduct of SIV; attends SIV.
May assist in and attends monitor visits and or audits.
May conduct site selection/qualification visits for potentially incoming clinical trials.
20% Data Coordinator Responsibilities (ex. May assist research coordinator in conduct of SIV; attends SIV; Enters data to complete forms (CRFs) on paper or in EDC)
