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