
Research and Development Professional
3 days ago
About the Role
This Senior Clinical Research Associate position plays a critical role in ensuring the success of our clinical trials. The successful candidate will have a proven track record in monitoring clinical trials, managing trial sites, and maintaining regulatory standards.
Key Responsibilities:
- Conduct site initiation visits, monitor clinical trials, and ensure compliance with protocol requirements.
- Develop and maintain effective relationships with site personnel, Investigators, and other stakeholders.
- Ensure accurate and timely reporting of trial data, including adverse events and protocol deviations.
- Collaborate with cross-functional teams to identify and implement process improvements.
- Supervise junior CRAs and provide guidance on best practices.
Requirements:
- Master's degree in a life science discipline or equivalent.
- Minimum 3 years of experience in clinical research, preferably in a CRO or pharmaceutical industry.
- Excellent communication, interpersonal, and problem-solving skills.
- Strong knowledge of GCP, ICH, and regulatory requirements.
- Ability to travel up to 50% of the time.
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