Senior Clinical Trial Associate
2 weeks ago
Roles and Responsibility
- Manage and coordinate clinical trial activities, including site monitoring and data management.
- Develop and maintain relationships with investigators, sites, and other stakeholders to ensure successful study execution.
- Conduct site visits and monitor clinical trials to ensure compliance with protocols and regulations.
- Collaborate with cross-functional teams to resolve issues and improve processes.
- Analyze data and prepare reports to support informed decision-making.
- Ensure timely and accurate communication with internal and external stakeholders.
Job Requirements
- Bachelor's degree in a related field (e.g., biology, pharmacy).
- Proven experience in clinical trials, preferably in a similar role.
- Strong knowledge of Good Clinical Practice (GCP) principles and regulatory requirements.
- Excellent communication and interpersonal skills.
- Ability to work independently and as part of a team.
- Strong analytical and problem-solving skills.
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