Clinical Project Manager Jobs in Michigan
A Clinical Project Manager in the biotechnology industry has the dynamic role of overseeing and orchestrating clinical trials. This includes developing trial protocols, coordinating with various departments and stakeholders, ensuring compliance with regulations, managing budgets, ensuring data accuracy, and liaising with regulatory authorities. This role is critical to ensuring the successful completion and analysis of clinical trials, which contribute to the development and approval of new biotechnology products. A Clinical Project Manager is also responsible for identifying and mitigating risks that could disrupt the trial timeline or compromise the data's validity.
For this role, a strong background in clinical trials, research, biotechnology, and project management is essential. A degree in life sciences or a related field is generally required, with advanced degrees or clinical research certifications being preferred. Key skills include attention to detail, problem-solving, leadership, and excellent communication skills. Certification as a Project Management Professional (PMP) can be beneficial. Prior to this role, an individual may have worked as a Clinical Trial Coordinator, Clinical Research Associate, or even as a Biostatistician, gaining valuable hands-on experience in clinical trials and research.
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
- 7 days ago
- Flint, MI
- 7 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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Salary for Clinical Project Manager Jobs in Michigan
Required or preferred licenses and certifications for Clinical Project Manager positions.
Highest Education Level
Clinical Project Managers in Michigan offer the following education backgroundQualifications / Skill Sets
The following top skills are often required or desired to land a Clinical Project 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
- Stem Cells
- 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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