长沙招聘

Job content (purpose of the job)
Key areas of responsibility:
Perform medical writing tasks
Be involved in publication planning of relevant products, including inputs and expertise, especially to data-driven related publication
Contribute to knowledge sharing, skill building and good collaboration with stakeholders and colleagues
Other areas of responsibility, if any
Main job tasks:
Perform medical writing tasks - including preparation of:
·Both English and Chinese versions of Clinical trial reports (CTRs) for CDP trials for registration purpose and English version for local trials
·Publications (abstracts, posters and slide presentations for conferences and other scientific meetings, and manuscripts for scientific journals) used to promote NN products
·Medical Writing assistance to top KOLs with their manuscript preparation for the domestic and international journals to maintain a good relationship with top KOLs and a scientific image of NN
·Clinical trial results presentations for distribution to clinical investigators
·Replies to questions from authorities
·Review of trial-related documents (Protocol, SAP, PCP, TVP, etc.) and non trial-related documents (SOP, MI magazine, etc.)
Be involved in publication planning of relevant products:
·Provide inputs to responsible products, especially for data-driven publication
·Provide expertise in target journal selection and scientific contents for data-driven publication as well as secondary publication
·Communicate with relevant internal and external stakeholders to ensure accepted abstract will be presented by appropriate person in the conference
Contribute to knowledge sharing, skill building and good collaboration with stakeholders and colleagues:
·Participate in internal/external marketing/medical activities, e.g., expert meetings, lectures and conferences
·Contribute to medical writing training for external stakeholders to maintain a good relationship with top KOLs and a scientific image of NN
·Contribute to process improvements
·Contribute to ongoing improvements in cross-functional and global collaboration and sharing of better practices and knowledge
·Maintain up-to-date knowledge and competencies within relevant therapeutic and professional areas
·Actively participate in relevant meetings, training sessions and seminars in the department, competency anchor and relevant project(s)
·Maintain a good working relationship with stakeholders and colleagues
Any other responsibilities and duties which may be required from time to time
Qualifications:(minimum requirements)
·Fluent English on both written & verbal
·Good writing skills for both Chinese and English
·Basic knowledge of biostatistics
·Good communication skills
·Ability and flexibility to plan and prioritise on complex tasks, multiple tasks and changing deadlines; to approach it business oriented.
·Ability to work effectively as a team player as well as independently
Education:
·Graduate (PhD of medical Sciences or clinical medicine or equivalent)
Professional experience:
·≥2 years of experience with scientific research methodology, including designing and conducting experiments, and analyzing and reporting experimental results
·Experience with scientific writing (publications in both Chinese and English journals or equivalent)
·Experience from the pharmaceutical industry is a major advantage but not a must
·Experience of project management is an asset

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