岗位职能：

• Act as medical expert on haematology/oncology for CBMG China for products in development and pipeline haematology/oncology products.
• To advise on haematology/oncology development issues for CBMG China Clinical Development and related line function units.
• To alert teams of advances and new data from global sources and local advances in haematology/oncology clinical sciences and treatment
• Develop or oversee CRO development of appropriate clinical trial protocols, synopses and clinical summaries.
• Discuss protocols with leading haematology/oncology specialists and related CBMG teams
• Provide strategic input to publications/publication plans, supervise writing, write and review abstracts, manuscripts for presentation/publication at internal/external meetings.
• Support IND and NDA clinical dossier preparation including clinical summaries etc.
• Support clinical operations teams by providing therapy area expertise and answer questions from clinical operations staff and/or site staff.
• Prepare, attend meetings and interact with Health Authority at specific meetings or on ad hoc basis. Provide expertise to cross-functional groups in preparations for HA interactions.
• Support decision regarding patient eligibility, enrolment and protocol deviation management

• Ensure regular contact with National Key Opinion leaders, visit on a regular basis and provide feedback to CBMG on scientific and treatment trends and also deliver key messages concerning the current CBMG and pipeline products.

• Participate in Advisory Boards, Symposia and Congresses to communicate latest data on CBMG therapies/pipeline products to appropriate physician audiences.
• Maintain an observant brief on pre-clinical haematology research institutes in China and inform CBMG of developments that may be of interest.

基本要求：

• Proven track record of clinical development in haematology/oncology and scientific achievements in clinical research.
• Advanced medical/scientific and state-of the art clinical research knowledge in haematology/oncology.
• Familiar with all aspects of the drug development process, including clinical trial design, protocol/CRF development, data analysis principles and clinical report writing.
• Proven ability to interpret, discuss and present efficacy and safety data in the haematology/oncology area internally and externally.
• 3-5 years experience in pharmaceutical industry clinical development experience in haematology/oncology area.
• Biomedical degree with specialism in haematology/oncology essential.

上班地址：浦东新区张江高科技园区法拉第路85号