Clinical Research Manager Jobs in Devens, 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.
Clinical Trial Manager (Senior)
- Watertown, MA (24 miles from Devens, MA)
- 2 hours ago
- Watertown, MA (24 miles from Devens, MA)
- 2 hours ago
guidelines, QC/QA procedures, as well as relevant clinical regulatory requirements Qualifications include : 5+ years of clinical trial operations experience in a biotech, pharmaceutical, CRO, clinical...
Clinical Research Project Manager
- Belmont, MA (23 miles from Devens, MA)
- 2 days ago
- Belmont, MA (23 miles from Devens, MA)
- 2 days ago
Site: The McLean Hospital Corporation Mass General Brigham relies on a wide range of professionals, including doctors, nurses, business people, tech experts, researchers, and systems analysts to...
Clinical Research Coordinator Acton, MA (Onsite)
- Acton, MA (9 miles from Devens, MA)
- 4 days ago
- Acton, MA (9 miles from Devens, MA)
- 4 days ago
research studies Must have analytical skill, be detail oriented and have good interpersonal skills Knowledge of global regulatory requirements and ICH guidelines Skills/Competencies: Excellent written...
- Watertown, MA (24 miles from Devens, MA)
- 7 days ago
- Watertown, MA (24 miles from Devens, MA)
- 7 days ago
Working knowledge of FDA, ICH-GCP, and international regulatory requirements. Prior involvement in IND or EU CTR submissions. Proficiency in common CTMS, eTMF, and EDC systems....
Clinical Project Manager (Hybrid)
- Acton, MA (9 miles from Devens, MA)
- 9 days ago
- Acton, MA (9 miles from Devens, MA)
- 9 days ago
Proactively stay abreast of the latest regulations and GCP (Good Clinical Practice) Support management of CRO and/or other outside clinical vendors. Co-manage study timelines and budgets....
- Waltham, MA (20 miles from Devens, MA)
- 11 days ago
- Waltham, MA (20 miles from Devens, MA)
- 11 days ago
Deep understanding of GCP, ICH guidelines, and regulatory frameworks relevant to global clinical trial management....
Clinical Research Coordinator II
- Worcester, MA (21 miles from Devens, MA)
- 12 days ago
- Worcester, MA (21 miles from Devens, MA)
- 12 days ago
Keep principal investigator and manager aware of any issues regarding compliance Comply with all safety and infection control standards appropriate to this position Adhere to Good Clinical Practice...
When you care deeply about the work you do, it's rewarding to see it through from concept to completion. We partner with clients to provide both program management and construction management to...
Senior Project Manager Life Sciences
- Watertown, MA (24 miles from Devens, MA)
- 18 days ago
- Watertown, MA (24 miles from Devens, MA)
- 18 days ago
Senior Project Manager Life Sciences Job ID 224838 Posted 13-Jun-2025 Service line PJM Segment Role type Full-time Areas of Interest Construction, Project Management Location(s) Brighton -...
RTSM Technical Project Manager/Business Systems Analyst Level I - Amendments (Hybrid Role)
- Wellesley, MA (23 miles from Devens, MA)
- 22 days ago
- Wellesley, MA (23 miles from Devens, MA)
- 22 days ago
Knowledge of US FDA Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) GCP regulations, Electronic Records; Electronic Signatures regulation (21 CFR Part 11) and EU Annex...
- Waltham, MA (20 miles from Devens, MA)
- 30+ days ago
- Waltham, MA (20 miles from Devens, MA)
- 30+ days ago
/GCP guidelines....
Remote WorkClinical Research Coordinator III
- Lowell, MA (17 miles from Devens, MA)
- 60+ days ago
- Lowell, MA (17 miles from Devens, MA)
- 60+ days ago
Review Board (IRB)....
- Waltham, MA (20 miles from Devens, MA)
- 60+ days ago
- Waltham, MA (20 miles from Devens, MA)
- 60+ days ago
Regulatory and Compliance Oversight: Ensure that clinical trials are conducted in compliance with all applicable regulations, including FDA, EMA, and ICH-GCP guidelines....
Clinical Research Coordinator I
- Andover, MA (24 miles from Devens, MA)
- 90+ days ago
- Andover, MA (24 miles from Devens, MA)
- 90+ days ago
The Role: Andover Eye Institute Per Diem, Clinical Research Coordinator I (CRC I) has close relationships with the subjects who participate in our clinical trials....
Demographic Data for Devens, MA
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Clinical Research Manager Online Courses and Training Opportunities
Title Synonyms
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Salary for Clinical Research Manager Jobs in Devens, MA
Required or preferred licenses and certifications for Clinical Research Manager positions.
Highest Education Level
Clinical Research Managers in Devens, MA offer the following education backgroundQualifications / Skill Sets
The following top skills are often required or desired to land a Clinical Research Manager position
- Institutional Review Board
- ICH GCP
- Study Management
- Clinical Monitoring
- Genomics
- Biomarkers
- Clinical Trial Management System
- Cancer Research
- Clinical Data Management
- Gene Therapy
- ICH Guidelines
- Good Clinical Practice
- Scientific Research
- Specimen Processing
- Drug Development
- Urine Testing
- Site Management
- Biotechnology
- Clinical Trials
- Clinical Research
- Clinical Operations
- Oncology
- Medical Device Sales
- FDA Regulations
- Phlebotomy
- Data Collection
- Public Health
- Standard Operating Procedures
- Patient Care
- Data Management
- Health Care
- Medical Terminology
- Collections
- Quality Control
- Auditing
- Investigation
- Written Communication
- Interpersonal Skills
- Quality Assurance
- Collaboration
- Education Experience
- Documentation
- Reporting
- Data Entry
- Bachelor's Degree
- Regulations
- Policy Development
- Microsoft Office
- Project Management
- Problem Solving
- Research Skills
- Microsoft Excel
- Staff Supervision
- Organization
- Scheduling
- Computer Skills
- Leadership
- Communication Skills
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