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 : CONSULTANT REGULATORY AFFAIRS
Job Description:
The candidate should be well versed in Regulatory Affairs with good experience in pre & post approval activities like renewals, variations, annual reports, change control assessment for global markets. Resource should also have experience in authoring and review of CMC sections and CMC documents and complication of dossiers for the one or two major regions among US, EU and ROW.
Also, he should be good in communication and writing skills and should be able to lead and train junior colleagues.
Experience in dealing and interacting with clients will be an added advantage.
Candidate Profile
First class Graduate/Post Graduate in Life Sciences/ Pharmacy with relevant work experience(RA) for 7-9 years in the reputed organizations.
Additional Information:
Experience: 7-9 years
Qualification : Graduate/Post Graduate in Life Sciences/ Pharmacy
Location: BENGALURU, KARNATAKA, INDIA
Industry Type: Pharma/ Healthcare/ Clinical research
Functional Area : REGULATORY AFFAIRS
End Date : 20th January, 2017
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