Mid-Level Clinical Trials Coordinator
5 days ago
About the Role
We are seeking a highly skilled Senior Clinical Trial Specialist to join our team. This individual will be responsible for providing operational support to ensure the successful execution of clinical trials, with a strong focus on ensuring compliance with GCP and regulatory requirements.
Main Responsibilities:
- Proactively identify and resolve operational project issues.
- Develop and implement process improvements to enhance clinical trial execution.
- Collaborate with cross-functional teams to ensure seamless execution of clinical trials.
- Provide expert guidance on GCP and regulatory requirements to study teams.
- Maintain accurate and up-to-date documentation of clinical trial activities.
Key Requirements:
- Bachelor's degree or equivalent combination of education/experience in science or a health-related field.
- Strong understanding of GCP, ICH, and knowledge of regulatory requirements.
- Minimum one year prior Clinical Trial Specialist experience or commensurate.
Estimated Salary: $100,000 - $120,000 per year
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