Clinical Trials Specialist
6 days ago
Job Overview: The Clinical Research Coordinator plays a critical role in the success of our clinical trials. As a member of our team, you will be responsible for managing the day-to-day activities of our studies, ensuring compliance with regulatory requirements, and providing exceptional customer service to our participants and stakeholders.
Key Responsibilities:
- Manage multiple clinical trials simultaneously, prioritizing tasks and meeting deadlines
- Develop and implement study protocols, standard operating procedures, and quality control measures
- Recruit and train study staff, including CRCs and monitors
- Conduct site initiation visits, monitoring visits, and close-out visits
- Maintain accurate records, including subject enrollment, payment, and milestones
- Compile and submit reports to the IRB, sponsor, and CRO
Qualifications:
- Minimum two years' experience in clinical research coordination
- Strong organizational and time management skills, with ability to work independently
- Excellent communication and interpersonal skills
- Ability to adapt to changing priorities and meet deadlines
What We Offer:
- Competitive salary range: $55,000 - $75,000 per year
- 19 days Paid Time Off
- 11 Paid Federal Holidays
- a 401(k) with a 5% company match
- Medical, Vision, & Dental insurance for Employees and Families- Employer paid at 70%
- Professional development training
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