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Site Management Specialist
3 weeks ago
This is an exciting opportunity for a skilled Clinical Research Associate to join our global team. As a CRA, you will be responsible for managing clinical trials at multiple sites, ensuring that studies are conducted in accordance with GCP and applicable regulations.
Key Tasks:
- Manage multiple clinical trials at various sites, ensuring timely completion and data quality.
- Conduct site initiation visits and ongoing monitoring visits to assess the quality of study conduct.
- Identify and escalate potential issues to the study team.
- Collaborate with investigators and site staff to resolve issues and improve study performance.
- Develop and maintain documentation related to site management and regulatory compliance.
Requirements:
- Bachelor's degree in a scientific or health-related field.
- Minimum 3 years of experience in clinical research, preferably as a CRA or SM.
- Strong understanding of GCP and regulatory requirements.
- Excellent communication and organizational skills.
- Ability to work independently and collaboratively as part of a team.
