Clinical Research Associate, Sponsor Dedicated
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Job Description
Clinical Research Associate managing study sites and monitoring compliance under GCP guidelines. Collaborating with project teams to enhance predictability and execute studies efficiently.
Responsibilities:
- Perform monitoring and site management work
- Conduct site monitoring visits in accordance with regulatory requirements
- Manage the progress of assigned studies by tracking submissions and approvals
- Ensure site documents are available for filing
- Collaborate and liaise with study team members
Requirements:
- 1-2 years of onsite monitoring experience
- Bachelor's Degree in scientific discipline or health care preferred
- Basic knowledge of GCP and ICH guidelines
- Proficiency in Microsoft Word, Excel, and PowerPoint
- Organizational and problem-solving skills
- Effective time and financial management skills
Benefits:
- health insurance
- retirement plans
- paid time off
- flexible work arrangements
- professional development opportunities
- bonuses
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