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 : Document Quality Reviewer
Job Description:
- Under departmental supervision, the Associate Medical Writer will prepare simple clinical documents.
- Perform edits and format changes on documents, as requested. Assist with final quality control check, compilation, formatting, tabulation, and pagination of documents.
- Prepare documents such as patient narratives, upfront/shell reports and complete study reports, under the supervision of the project lead Medical Writer.
- Excellent interpersonal, verbal and written communication skills.
- Client focused approach to work.
- A flexible attitude with respect to work assignments and new learning.
Candidate Profile
Graduate or Postgraduate in Life Sciences. Scientific background essential. Some experience of medical writing of regulatory documents such as patient narratives, informed consent forms or similar in a contract research organization, pharmaceutical or biotechnology firm, or some experience in the conduct of clinical research/medical communications.
Additional Information:
Location: Bengaluru
Education: Graduate or Postgraduate in Life Sciences
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: Reviewer
Job ID : 40006BR
End Date: 18th January, 2018
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