Clinical Trial Manager Jobs in High Point, NC
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.
- Greensboro, NC (14 miles from High Point, NC)
- 10 days ago
- Greensboro, NC (14 miles from High Point, NC)
- 10 days ago
Research program, ensuring adherence to standards for good clinical practice (GCP) and compliance with guidelines and regulations from the office of Human Research Protection (OHRP), the Food and Drug...
Clinical Research Coordinator II
- Greensboro, NC (14 miles from High Point, NC)
- 10 days ago
- Greensboro, NC (14 miles from High Point, NC)
- 10 days ago
Supports the regulatory process in the submission of study protocols, consent forms, and recruiting materials to the Institutional Review Board and the department for approval, facilitating the regulatory...
- Greensboro, NC (14 miles from High Point, NC)
- 27 days ago
- Greensboro, NC (14 miles from High Point, NC)
- 27 days ago
Supports the regulatory process in the submission of study protocols, consent forms, and recruiting materials to the Institutional Review Board and the department for approval, facilitating the regulatory...
Project Manager I, Biomedical Engineering
- Winston Salem, NC (16 miles from High Point, NC)
- 45+ days ago
- Winston Salem, NC (16 miles from High Point, NC)
- 45+ days ago
Prior experience with clinical trials strongly preferred. Supervisory ability. Master's degree in a relevant discipline with experience beyond three years preferred....
LL02-012225 Project Manager for Biotech Laboratory Operations
- High Point, NC
- 45+ days ago
- High Point, NC
- 45+ days ago
Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the...
LL01-012225 Project Manager for Biotech Operation Readiness
- High Point, NC
- 45+ days ago
- High Point, NC
- 45+ days ago
Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the...
Demographic Data for High Point, NC
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Salary for Clinical Trial Manager Jobs in High Point, NC
Required or preferred licenses and certifications for Clinical Trial Manager positions.
Highest Education Level
Clinical Trial Managers in High Point, NC 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
- 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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