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Medical Safety writers play a very important role at every stage of Drug Development process. They are the most demanding professionals in PV sector. Companies require highly skilled personnel for understanding & writing safety reports. The work done should be accurate and within the timeframes provided. Scope of the Job starts from Clinical Development stage to the post marketing and surveillance activities. Medical writing is an integral part of every stage. Therefore a high demand of writers for successful submission of Regulatory documents is generated from time to time in the industry.
• Fresher Level job in Pharmacovigilance is DSA (Drug Safety Associate). A Drug safety Associate is mainly involved in case creation, checking for MSI (Minimum safety information - a patient, a reporter, a suspect drug and a adverse event), reconciliation and follow up process, data entry of all information available in the document and medical coding
• 3 Years of experience builds more skill sets as (Medical coding, narrative and scientific writing, good understanding of medical terms and basic understanding of regulatory affairs, ICH-GCP and compliance etc) which can bag him a position as DSS (Drug Safety Scientist).
• With a Certification in Pharmacovigilance and an overall of 5+ Years experience, candidates can become a Team lead or Team manager based on the company.
Students can download the admission form by clicking here, in PDF format print and fill the same, clearly mentioning Mobile No & Course Interested.