PAREXEL has supported the Bio-Tech and Pharmaceutical industries in helping the development of new drugs and treatments on a global basis. As a leading global biopharmaceutical service provider, they supply knowledge-based contract research, medical communications and consulting services across a broad range of therapeutic areas to the worldwide pharmaceutical, biotechnology and medical device industries. They have helped over 800 clients to develop and launch some of the most important drugs and devices of our time-helping people live better and healthier lives everywhere in the world. Headquartered near Boston, Massachusetts, PAREXEL operates in more than 50 countries around the world.
Post : Associate-Evidence Evaluation
Job Description
Key Accountabilities
• 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
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• 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.
• Prior experience in client interaction 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
Additional Information:
Location: Chandigarh
Education: B.Pharm/M.Pharm/M.Sc/Phd (Life Sciences)
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: Evidence Evaluation
End Date: 18th December, 2017
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