Our client is a global medical company using technology to analyse and predict disease risks, with an approved medical device platform.
Responsibilities
- Oversee all aspects of clinical research.
- Supervise on-site clinical studies, ensuring they meet timelines.
- Maintain thorough documentation and work closely with local investigators.
- Provide feedback to cross-functional teams and assist in product development.
Qualifications
- Bachelor's degree in a relevant healthcare field.
- Minimum of 3 years of experience managing clinical trials independently, preferably in the medical device sector.
- Knowledge of medical device clinical trial design and MFDS regulations.
- Excellent communication skills.
- Willing to travel.
If you are interested, please apply with your CV attached.
