Clinical Trial Manager Jobs in Michigan
A Clinical Trial Manager in the biotechnology industry oversees the planning, implementation, and completion of clinical trials. They are crucial in ensuring that trials are conducted in a way that ensures patient safety, data integrity, and regulatory compliance. They manage budgets, timelines, resources, vendors, and staff involved in the clinical trial, and also handle data management and reporting. They are also responsible for protocol development, site management, and monitoring the study's progress by coordinating with the clinical research associates.
Key skills for a Clinical Trial Manager include strong leadership, project management, and communication abilities. They should also be proficient in medical terminology and have a strong understanding of Good Clinical Practices (GCP), as well as FDA and ICH regulations. A degree in life sciences, nursing or related field, certification like Certified Clinical Research Professional (CCRP) or Certified Clinical Data Manager (CCDM) are often required. Prior roles before becoming a Clinical Trial Manager might include Clinical Research Associate, Clinical Data Coordinator, or Clinical Project Coordinator.
Knowledgeable of all types of clinical trials to assure that the applicable regulations are considered....
Coordinator Clinical Research Senior - PART TIME - McLaren Careers
- Flint, MI
- 8 days ago
- Flint, MI
- 8 days ago
Qualifications: Required: Associate degree in science or other clinical area Five or more years of experience as a clinical research coordinator Clinical Research Certification through SOCRA or ACRP...
Manages participant engagement throughout clinical trials by identifying eligible subjects, conducting informed consent processes, coordinating reimbursement, verifying eligibility, and serving as the...
Qualifications: Required: Associate degree in science or other clinical area Five or more years of experience as a clinical research coordinator Clinical Research Certification through SOCRA or ACRP...
Clinical Research Coordinator - Pediatric Hematology and Oncology - Kalamazoo
- Kalamazoo, MI
- 11 days ago
- Kalamazoo, MI
- 11 days ago
Education in the protection of human research participants and Good Clinical Practices required Current clinical licensing and board certification required, if applicable....
-Complete all relevant Profound Research required training, including but not limited to ICH-GCP certification and IATA certification in a timely manner....
Communicate with study sponsors, research team and the Institutional Review Board....
Practice (ICH GCP)....
Sr. Manager, Project Manager / Program Manager
- Grand Rapids, MI
- 30+ days ago
- Grand Rapids, MI
- 30+ days ago
Quality, Service, Collaboration, Courage. Do you exhibit these values and wish to be around others that do too? Are you interested in making a difference in your community and the world? Are you...
Monitor day-to-day study conduct to ensure protocol, SOP, and Good Clinical Practice compliance. Review and create trial forms to ensure protocol compliance....
Clinical Research Coordinator - Department of Psychiatry
- Detroit, MI
- 90+ days ago
- Detroit, MI
- 90+ days ago
Clinical Research Coordinator - Department of Psychiatry Wayne State University is searching for an experienced Clinical Research Coordinator - Department of Psychiatry at its Detroit campus location...
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Title Synonyms
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Salary for Clinical Trial Manager Jobs in Michigan
Required or preferred licenses and certifications for Clinical Trial Manager positions.
Highest Education Level
Clinical Trial Managers in Michigan offer the following education backgroundQualifications / Skill Sets
The following top skills are often required or desired to land a Clinical Trial Manager position
- Budgets
- ICH GCP
- Institutional Review Board
- Clinical Trial Management System
- Study Management
- Clinical Monitoring
- Biomarkers
- Clinical Data Management
- Gene Therapy
- ICH Guidelines
- Good Clinical Practice
- Cancer Research
- Medical Affairs
- Scientific Research
- Drug Development
- Site Management
- Biology
- Immunology
- Clinical Trials
- Neuroscience
- Biotechnology
- Clinical Operations
- Clinical Research
- Oncology
- FDA Regulations
- Medical Device Sales
- Public Health
- Data Collection
- Patient Care
- Standard Operating Procedures
- Data Management
- Phlebotomy
- Health Care
- Medical Terminology
- Affirmative Action
- Collections
- Military Background
- Investigation
- Auditing
- Presentation
- Written Communication
- Documentation
- Collaboration
- Data Entry
- Bachelor's Degree
- Reporting
- Education Experience
- Regulations
- Policy Development
- Project Management
- Research Skills
- Microsoft Office
- Microsoft Excel
- Problem Solving
- Time Management
- Staff Supervision
- Organization
- Scheduling
- Computer Skills
- Leadership
- Communication Skills
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