Clinical Trial Manager Jobs in Marquette, MI
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.
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Demographic Data for Marquette, MI
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Title Synonyms
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Salary for Clinical Trial Manager Jobs in Marquette, MI
Required or preferred licenses and certifications for Clinical Trial Manager positions.
Highest Education Level
Clinical Trial Managers in Marquette, MI offer the following education backgroundQualifications / Skill Sets
The following top skills are often required or desired to land a Clinical Trial Manager position
- Budgets
- Institutional Review Board
- ICH GCP
- Study Management
- Clinical Monitoring
- Genomics
- Clinical Trial Management System
- Biomarkers
- Cancer Research
- Gene Therapy
- ICH Guidelines
- Good Clinical Practice
- Medical Affairs
- Biostatistics
- Scientific Research
- Drug Development
- Biology
- Site Management
- Clinical Trials
- Biotechnology
- Clinical Operations
- Clinical Research
- Neurology
- Oncology
- Medical Device Sales
- FDA Regulations
- Phlebotomy
- Data Collection
- Public Health
- Patient Care
- Standard Operating Procedures
- Data Management
- Medical Terminology
- Health Care
- Collections
- Quality Control
- Investigation
- Auditing
- Presentation
- Written Communication
- Documentation
- Collaboration
- Interpersonal Skills
- Bachelor's Degree
- Data Entry
- Education Experience
- Regulations
- Reporting
- Policy Development
- Project Management
- Problem Solving
- Research Skills
- Microsoft Office
- Microsoft Excel
- Staff Supervision
- Organization
- Scheduling
- Computer Skills
- Leadership
- Communication Skills
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