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Rachit Sharma
Drug Safety Senior Scientist
Drug Safety Senior Scientist
Rachit Sharma is a Senior Drug Safety / Pharmacovigilance professional with over 13 years of experience in global case processing, regulatory submissions, SAE management, narrative writing, and quality control. He has extensive hands-on expertise using Argus and Arisg databases, SAE reconciliation, MedDRA coding, and e2b transmission workflows. Rachit consistently delivers high-quality, audit-ready safety deliverables, while ensuring compliance with regulatory timelines and global pharmacovigilance requirements. Known for her analytical approach, leadership capability, and strong documentation skills, He excels in handling complex safety cases, training team members, and driving process improvements.
FORMERLY AT
Accenture Pharma Services
LOCATION
Chennai
AVAILABILITY
Full-time
Skills
Argus
ARISg
MedDRA
MedDRA Coding
MS Office
Safety Databases (Argus/Arisg)
SQL/PL-SQL
Work Experience
Drug Safety Senior Scientist
Accenture Pharma Services
November 2012 – Present
- Manage end-to-end adverse event case processing including collection, follow-up, evaluation, and regulatory reporting for clinical and post-marketing safety cases.
- Prioritize case handling to meet global submission timelines.
- Perform data entry, MedDRA coding, quality review, and narrative writing in Argus/Arisg.
- Handle e2b submissions, post-lock corrections, and SAE reconciliation.
- Monitor potential safety signals and assist in team training for PV processes.
TECHNOLOGIES
Argus, Arisg, SQL/PL-SQL, MedDRA
QC Associate
Synowledge PV Services
January 2012 – November 2012
- Conducted quality control of safety cases and ensured compliance with global reporting standards and SOPs.
TECHNOLOGIES
Safety Databases (Argus/Arisg), MedDRA Coding
Safety Processing Expert
Novartis Healthcare
June 2011 – December 2011
- Supported global pharmacovigilance case processing activities including data entry, coding, and documentation.
TECHNOLOGIES
Argus, Arisg, MS Office
