Clinical Research Coordinator

4 weeks ago


Los Angeles, California, United States Amerit Consulting Full time

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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