| Major Responsibilities:
-Gather plans and budgets for Post Marketing Trials from brand teams for input into the APRMA budgeting and planning process -Liaise with Regional GDMA QA on local SOP, clarifying needs on local SOP and/or translation -Review and tracking local operating expense on medical activities and clinical studies -Develop and maintain contacts with Expert physician, in accordance with the strategy developed by the Company to further understand and gain both insight and/or input into medical activities, including (1) the clinical research activities and (2) the needs and behaviours of health care providers. -Encourage the participation, as required and as appropriate, of Physicians in local studies and other scientific activities -Work with DAH/DAS/RDMLs and GDO to review local/regional protocols, set local recruitment targets and contribute to site selection, in brands where DAS/MSM is not available -Collect investigators’ proposals for local and regional clinical activities, ensure that these proposals are discussed within the local Brand Team, manage internal and external approval processes, and provide timely feedback to investigators, in brands where DAH/DAS/MSM is not available -Maintain the IST-related documents, from initial request to approval, in the appropriate binder -Ensure the appropriate input of the medical plan into GMAST -Provide support to GDO on medical activities relating to the conduct of a trial or survey -Provide oversight to progress of the company-sponsored/supported study activities through IMPACT -Ensure that local regulation and BMS Pharmacovigilance SOPs are understood and applied by Investigators, and alert appropriate BMS personnel to any Adverse Events that are identified -Adhere to the country specific “Code of Conduct”, and alert management to possible compliance issues -Convey a clear message on legal and ethical standards to Expert Physicians and Investigators -Develop and maintain a good understanding of SOPs, GCP and ICH, if appropriate, as well as legal and ethical standards Qualification Requirement: -Knowledge of clinical trial design and process -Knowledge of the National Healthcare System and the pharmaceutical industry -Good English language skills, spoken and written -Word, PowerPoint and Excel skills -Working in a scientific and/or clinical research environment -Quickly and comprehensively learning about new subject areas and environments If you are interested in this job, please be free to contact us by teachcn@yahoo.com.cn or cn.hr@bms.com |
