The Clinical Project Associate will be responsible for
- Management of activities for our clinical research studies, including protocol development, regulatory submission, engagement of clinical service providers, developing and keeping of timelines.
- Preparation and maintenance of clinical trial documentations, as well as management of scientific collaborations.
- Assisting on existing projects, in terms of problem solving and liaison with clinicians, CROs, statistician and logistic provider.
- Miscellaneous administrative tasks assigned by supervisor.


Basic requirements for the role include:
- Possess a Bachelor’s degree in Life sciences/pharmacy/related discipline.
- Excellent communication, organizational and planning skills.
- Demonstrated ability to manage multiple tasks with positive attitude and prioritize workload with attention to details.
- Ability to read and write Chinese will be a plus.