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Clinical Research Site Manager
2 months ago
Job Summary
The Clinical Research Site Manager is responsible for ensuring the successful execution of clinical trials at assigned investigative sites. This includes ensuring compliance with sponsor protocols, FDA regulations, and ICH/GCP guidelines, as well as providing high-quality data to sponsors.
Key Responsibilities
- Compliance and Quality Assurance
- Ensure compliance with sponsor protocols, FDA regulations, and ICH/GCP guidelines
- Conduct regular site visits to monitor compliance and quality
- Study Management
- Oversee the management of clinical trials at assigned sites
- Ensure timely and accurate data collection and reporting
- Staff Management
- Supervise and train site staff on clinical trial procedures and protocols
- Ensure staff are aware of and comply with company policies and procedures
- Communication and Collaboration
- Communicate effectively with sponsors, site staff, and other stakeholders
- Collaborate with cross-functional teams to ensure successful trial execution
- Problem-Solving and Decision-Making
- Identify and resolve issues related to trial execution
- Make informed decisions to ensure trial success
Requirements
- Education
- Bachelor's degree in a related field (e.g. life sciences, healthcare)
- Experience
- At least 4 years of experience in clinical research, including 2 years of management experience
- Credentials
- Certified Clinical Research Coordinator (CCRC) or equivalent certification
- Skills
- Strong teamwork, organizational, and problem-solving skills
- Excellent communication and interpersonal skills
- Ability to multitask and work in a fast-paced environment
Working at DM Clinical Research
At DM Clinical Research, we are committed to delivering high-quality clinical trials that meet the needs of our sponsors and patients. We are seeking a highly motivated and experienced Clinical Research Site Manager to join our team.