Clinical Research Manager Jobs in Plymouth, MA
A Clinical Research Manager plays a pivotal role in the biotechnology industry by overseeing and managing clinical trials. They are responsible for creating and implementing trial protocols, ensuring compliance with legal and ethical standards, coordinating with various internal and external stakeholders, and overseeing data collection, management, and analysis. They also monitor the progress of clinical studies and ensure they are completed on time and within budget, while maintaining patient safety and data integrity.
Key skills and certifications for this role include a robust knowledge of Good Clinical Practice (GCP) guidelines, strong analytical and project management skills, and excellent communication abilities. A Clinical Research Manager may also need certifications such as Certified Clinical Research Professional (CCRP) or Certified Clinical Research Coordinator (CCRC). Prior to becoming a Clinical Research Manager, an individual might have roles such as Clinical Research Associate or Clinical Research Coordinator, which provide the essential experience in clinical trial conduct and management.
Experience performing clinical assessments, including but not limited to obtaining vital signs, EKGs, blood draws, processing/shipping lab specimens Experience with CRIO (Clinical Trial Management System...
Demographic Data for Plymouth, MA
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Title Synonyms
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Salary for Clinical Research Manager Jobs in Plymouth, MA
Required or preferred licenses and certifications for Clinical Research Manager positions.
Highest Education Level
Clinical Research Managers in Plymouth, MA offer the following education backgroundQualifications / Skill Sets
The following top skills are often required or desired to land a Clinical Research 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
- Neuroscience
- Clinical Trials
- 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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