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.
Post : Drug Safety Associate
Job Description
• Responsible for capturing and assessing single adverse event reports associated with client products on the client’s Drug Safety database, in accordance with client and applicable regulatory requirements
• Performing clear and accurate data capture/entry of case including book-in, completion of data entry of all fields on the basis of information provided in source documents, case assessment, coding of patient history, concomitant medications, event and drug terms using embedded dictionaries using Argus & & writing narratives
• Performing self QC of the case
• Ensuring MedRDA coding in accordance with “MedRDA Term Selection: points to consider” where applicable
Candidate Profile
• Health Professional (Masters in Pharmacy/Bachelor of Dental Surgery)
• Masters in Life Science (Microbiology/Biotechnology/Human Genomics/Biochemistry etc)
• Work with Web-based applications and familiarity with Windows Operating System and MS office suite (Word/Excel/Power Point)
• Capability to make concise, accurate and relevant synopsis of medical text and data, and the ability to write unambiguous medical text.
Additional Information
Job ID : 54212BR
Qualification : B.Pharm, B.Sc
Location : Mohali, Punjab
Industry Type : Pharma / Healthcare / Clinical research
Functional Area : Drug Safety
End Date : 25th September, 2019
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