天津招聘

POSITION SUMMARY

? Be responsible for planning, writing, and management of clinical trial reports, submissiondocuments , and other clinical documents. Providing critical input to the analysis and interpretation of clinical data. 

? Supporting organization to build and Lead a team of medical writers , including management and provision of training and coaching. Broadening the scope of the medical writing function and contribute to its development

ACCOUNTABILITIES: 

 

The responsibilities of the Medical Writer include, but are not limited to: 

 

? Write high-quality clinical documents in collaboration with international study and project teams. This includes planning , development of document strategies , document coordination , overseeing of timelines , and contribution to related clinical documents (e.g. study protocols,

analysis plans, statistical outputs, mock documents , investigator brochures) . 

? Ensure timeliness and quality of assigned medical writing projects, using both internal and external resources. 

? Supervise and provide training and coaching to team members.

? Develop, adhere to, and improve medical writing standards; ensure compliance .

? Enhance cooperation with other functions and other medical writing groups. Increase

awareness and understanding of medical writing and broaden the scope of the medical writing function. 

? Continuous awareness of latest regulatory guidelines for clinical document. Ensure appropriate maintenance of training records of team members. 

QUALIFICATIONS. EXPERIENCE & SKILLS 

 

?  Master  Degree    or  equivalent   experience  ;  Major  in  Biology  I  Medicine  I Pharmaceutics . 

? Fluent in written and spoken English. A second language will be an advantage .

? Basic medical knowledge; Sound understanding of the clinical development  process; Good understanding of statistics and pharmacokinetics ; Excellent scientific and analytical thinking ;

? Ability to comprehend and interpret clinical data; Excellent writing skills; Ability to write documents according to readers' expectations ; Outstanding capacity to structure text and data in a clear and concise fashion .

? Ability to lead and motivate people; Excellent communication and interpersonal skills .

? Efficient time and project management skills.

? Proficiency in word processing and presentation software

 

We are a global provider of consulting, and outsourced development and commercialisation services to pharmaceutical, biotechnology, medical device and government and public health organisations. We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas. ICON has been recognised as one of the world’s leading Contract Research Organisations through a number of high-profile industry awards.