Responsibilitie********
Design an******** clinical trial********
Lead an******** of communication strategies to support existingan******** studies including KOL ******** advisory boar******** majormedical meet******** congresses an******** events, publicationsan******** materials.
Manage safety/PV an******** integrity of clinical trials.
Prepare variety of medically-relate******** an******** wr********including Investigator Brochures, Protocals, reports for INDs, CTAs,etc.
With ability to collaborate an******** with Regulatory AffairDepartments regarding to regulatory submissions an******** adverseevents report******** as required.
Contribute science input into relavent therapeutic/disease areastrategy.
Respresents company at scientific an******** meetings as required.
Collaborate with variety of internal an******** partners, such ascl******** sc******** business ******** etc.
Requiremen********
Minimum MD or MD/PHD
Minimum 5 years experience in design an******** clinical trials inOncology.
Open-m******** fasting learning an********.
Team-worker.
Fluency in written an******** Chinese/English.