My client is a Oncology focused biotechnology company and currently seeking a dedicated and experienced Medical Doctor. The ideal candidate will play a crucial role in evaluating clinical trial protocols, ensuring patient safety, and contributing to the advancement of medical research, particularly in the field of oncology.
Key Responsibilities:
- Review and assess clinical trial protocols, informed consent documents, and study reports for compliance with regulatory standards and ethical guidelines.
- Collaborate with research teams to provide expert insights on oncology-related trials.
- Monitor patient safety and data integrity throughout the clinical trial process.
- Participate in meetings with regulatory bodies and stakeholders to discuss trial findings and recommendations.
- Contribute to the development of clinical trial strategies and methodologies.
- Stay updated on the latest advancements in oncology and clinical research.
Qualifications:
- Medical degree (MD) and current registration as a medical doctor in South Korea.
- Significant experience in oncology
- Proven experience in clinical trials
- Strong analytical and critical thinking skills.
- Excellent communication and collaboration abilities.
- Ability to work in a fast-paced, multidisciplinary environment.
If you are interested, please apply with your CV attached.
