Clinical Trial Manager Jobs in Tennessee
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.
research within biotech, pharma or CRO industry Proven experience in clinical research including relevant experience as team lead in clinical functions Experience as CRA is preferred Travel: Travel...
Clinical Research Coordinator II - Heart Valve Research (Term Position)
- Nashville, TN
- 3 days ago
- Nashville, TN
- 3 days ago
Assures research information is collected and stored in a manner that is compliant with regulations/policies and good clinical practice....
Immunology clinical trials....
integrity and quality of the research is maintained and that the research is conducted in accordance with Good Clinical Practice Guidelines, federal and sponsor regulations and guidelines, VUMC policies...
Clinical Research Coordinator I, Hematology/Oncology
- Nashville, TN
- 7 days ago
- Nashville, TN
- 7 days ago
Assures research information is collected and stored in a manner that is compliant with regulations/policies and good clinical practice....
The Clinical Research Coordinator II (CRC II) will be responsible for coordinating advanced clinical research projects proficiently with supervision....
Description JR Automation, a Hitachi Group Company, is driven to deliver customer success worldwide. We provide intelligent automated manufacturing and distribution technology solutions that...
and clinical research regulations (ICH-GCP, IRB processes, FDA regulations) Ability to identify and escalate critical issues to PI, IRB, or supervisors Strong organizational and communication skills...
The Clinical Research Coordinator will be responsible for the administrative duties and coordination efforts required in a medical research program....
Required Skills 1+ year of clinical research experience. Pre-screening patients for clinical trials. Expertise in clinical research and patient recruitment....
The CRC I will assist with the operational and financial functions of the Clinical Research....
The CRC I will assist with the operational and financial functions of the Clinical Research....
visits, patient screening, accrual and follow-up, informed consents, monitor visits, case report form submissions, and reporting of severe adverse events Assure adherence to SOPs, good clinical practice...
The CRC I will assist with the operational and financial functions of the Clinical Research....
The Clinical Research Coordinator II (CRC II) will be responsible for coordinating advanced clinical research projects proficiently with supervision....
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Title Synonyms
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Salary for Clinical Trial Manager Jobs in Tennessee
Required or preferred licenses and certifications for Clinical Trial Manager positions.
Highest Education Level
Clinical Trial Managers in Tennessee offer the following education backgroundQualifications / Skill Sets
The following top skills are often required or desired to land a Clinical Trial Manager position
- Report Generation
- ICH GCP
- Institutional Review Board
- Study Management
- Clinical Monitoring
- Genomics
- Biomarkers
- Clinical Trial Management System
- Cancer Research
- Gene Therapy
- Good Clinical Practice
- ICH Guidelines
- Biostatistics
- Scientific Research
- Specimen Processing
- Urine Testing
- Drug Development
- Site Management
- Medical Writing
- Biotechnology
- Clinical Trials
- Clinical Research
- Clinical Operations
- Neurology
- Oncology
- FDA Regulations
- Phlebotomy
- Data Collection
- Public Health
- Patient Care
- Standard Operating Procedures
- Data Management
- Health Care
- Medical Terminology
- Collections
- Military Background
- Auditing
- Investigation
- Education Experience
- Interpersonal Skills
- Quality Assurance
- Collaboration
- Documentation
- Reporting
- Data Entry
- Policy Development
- Bachelor's Degree
- Regulations
- Microsoft Office
- Project Management
- Problem Solving
- Research Skills
- Microsoft Excel
- Staff Supervision
- Organization
- Scheduling
- Computer Skills
- Leadership
- Communication Skills
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