Pharmacovigilance-Regulatory affairs @ accenture ,
Any Graduate
Job Skill: Regulatory affairs
Designation: Career Level - 11-Analyst
Job Location: Hyderabad
Qualifications: Any Graduation
Years of Experience: 3-5 years
About Accenture
Accenture
is a leading global professional services company, providing a broad range of
services and solutions in strategy, consulting, digital, technology and
operations. Combining unmatched experience and specialized skills across more
than 40 industries and all business functions —underpinned by the world’s
largest delivery network — Accenture works at the intersection of business and
technology to help clients improve their performance and create sustainable
value for their stakeholders. With 482,000 people serving clients in more than
120 countries, Accenture drives innovation to improve the way the world works
and lives. Visit us at www.accenture.com
Job Summary
You will be aligned with our
Pharmaceuticals Processes vertical and help us with the processes to collect,
monitor, research, assess and evaluate information on the adverse effects of
medication with a view to identifying new information about hazards associated
with medicines and consequently, prevent harm to patients. It also deals with
the reviewing and resolving of discrepancies identified by the system or
through manual checks as per guidelines. Employees under this span can also be
responsible for a number of activities related to the design, development, and
maintenance of Clinical Database objects.
You will be working as a part of
Pharmacovigilance team which designs and maintains a safety database to monitor
single case support activities; source distribution for business partners and
to perform medical literature searches. Responsible for data entry, MedDRA
coding and label assessment of adverse event in SUSAR cases. If there are issues
with the provided information, scientist is contacted for verification.
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