- Previous experience in Investigator Initiated Trials
- Ability to interpret and ensure protocol adherence
- Minimum 3-5 years of hands-on experience in clinical trials
- Coordinate and schedule study visits, ensuring availability of necessary supplies and investigator
- Provide personalized education to subjects and families, ensuring consent is obtained and specimens are collected
- Serve as a key link between Sponsor, Investigator, and Study Subjects
- Collect and manage study data accurately and in a timely manner
- Maintain study documents in compliance with relevant regulations and guidelines
- Work with Investigator to identify and report adverse events promptly to ensure subject safety
- Deliver excellent customer service to internal and external stakeholders
- Adhere to all regulatory requirements and policies
- Demonstrate expertise in federal and state regulations governing clinical trials
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Clinical Research Coordinator - Phoenix, United States - Medasource
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Description
Clinical Research Coordinator Job Opening
Start Date: Immediate, with flexibility
Contract Type: 6-month contract with the potential for full-time hire
Location: Onsite in Phoenix, AZ
Interview Process: 2 Rounds
Essential Qualifications:
Main Responsibilities: