Job Description
• Review scientific evidence emerging from clinical efficacy and safety studies
• Develop, run and validate literature searches for efficacy and adverse event data
• Analyse evidence based on standard network meta-analysis techniques
• Development of evidence based reports on clinical efficacy and safety to support reimbursement and regulatory requirements
• Independently work on a range of scientific deliverables ranging from abstracts, to detailed reports following a clear, concise and scientific style with attention to detail on the depth of the scientific content
• Ensure deliverables meet Parexel quality or best practice standards in medical writing of accuracy, clarity and neatness
• Communicate project outcomes clearly and concisely both internally and externally to the clients with support from project managers.
• The production of systematic literature reviews, through the analysis of large volumes of qualitative and quantitative health care data, combined with the ability to interpret the information in a meaningful way.
• Development of a range of scientific deliverables ranging from abstracts, manuscripts to review reports following a clear, concise and scientific style with attention to detail on the depth of the scientific content.
• Production of internal deliverables/working documents including protocol and ensuring that the documents are of the highest quality standards
• Ensuring deliverables meet HERON quality or best practice standards in medical writing
• Participation in Client calls and discussion of project related aspects
• Application of medical statistics and meta-analytical techniques to analyze and interpret data.
Skills
• Excellent interpersonal, verbal and written communication skills
• Client focused approach to work
• A flexible attitude with respect to work assignments and new learning
• Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail
• Willingness to work in a matrix environment and to value the importance of teamwork.
• Strong writing skills in terms of clear, accurate and concise scientific content writing;
• Demonstrated track record of quality publications, presentations, and research or prior experience in medical content writing.
• Prior experience in client interaction will be preferred
• Hands on knowledge of computers especially Microsoft Excel & Microsoft Word
• Recognized Post graduate or PhD degree in Pharmacy/ life sciences
• Excellent knowledge and preferably experience with a Pharma- KPO/ Pharmaceutical company
• Strong writing skills in terms of clear, accurate and concise scientific content writing; demonstrated track record of quality publications, presentations, and research or prior experience in medical content writing. Experience in health outcomes research will be preferred.
• Good knowledge of bio statistics
• Hands on knowledge of computers especially Microsoft Excel & Microsoft Word
• Good verbal & written English Communication skills
• Go getter mind-set with the ability to achieve the objectives set out by the management
• Methodical & Meticulous approach
• Process orientation
• Delivery focus
• High energy levels
• Passion for excellence
• Quality mind-set
Location: Chandigarh
Education: M.Sc/M.Pharm/BDS/PhD
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: Evidence Evaluation
Job ID : 42854BR
End Date: 18th March, 2018
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