Clinical Research Coordinator
4 weeks ago
Job Title: Clinical Research Coordinator - Regulatory Specialist
Job Summary:
Amerit Consulting is seeking an experienced Clinical Research Coordinator - Regulatory Specialist to join our team. The ideal candidate will have a strong background in regulatory affairs and clinical trials, with a proven track record of success in coordinating studies and ensuring compliance with regulatory requirements.
Key Responsibilities:
- Coordinate clinical trials from start-up to close-out, ensuring compliance with regulatory requirements and study protocols.
- Develop and maintain strong relationships with investigators, research sites, and other stakeholders to ensure successful study execution.
- Prepare and submit regulatory documents, including IRB applications and study protocols.
- Conduct site initiation visits and monitor study progress to ensure compliance with regulatory requirements.
- Collaborate with cross-functional teams to identify and mitigate study risks and ensure successful study execution.
Requirements:
- At least 1 year of experience in regulatory affairs and clinical trials.
- Strong knowledge of regulatory requirements and study protocols.
- Excellent communication and interpersonal skills.
- Ability to work independently and as part of a team.
What We Offer:
- A dynamic and supportive work environment.
- Opportunities for professional growth and development.
- A competitive salary and benefits package.
Amerit Consulting:
Amerit Consulting is a fast-growing staffing and consulting firm that provides consulting, temporary staffing, direct hire, and payrolling services to Fortune 500 companies and small to mid-sized organizations. We are committed to delivering exceptional service and results to our clients and employees.
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