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Pharmacovigilance Jobs in India
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Pharmacovigilance • India
Pharmacovigilance Services Associate
myGworkBengaluru, IndiaDir Pharmacovigilance
Teva PharmaceuticalsBangalore, IndiaSolution Lead - Pharmacovigilance
ArisGlobalKA, INManager - Pharmacovigilance Department
Jeevan Scientific Technology LimitedINDIATeam Lead, Pharmacovigilance Safety System
BaxterBengaluru, KarnatakaExecutive Pharmacovigilance
Piramal GroupMumbai, Maharashtra, IndiaPharmacovigilance Manager
PATHIndia, New Delhi Country Program OfficeExecutive-Pharmacovigilance / RA
Boyen Haddin Consultants LLPINDIAAssoc Dir, Pharmacovigilance
IQVIAINDIAPharmacovigilance Tester (Argus Safety)
IQVIA IndiaBengaluru, Karnataka, IndiaPharmacovigilance QC Team Lead
SanofiHyderabadGeneral Manager Pharmacovigilance
WHYFLEX HUMAN CAPITALINDIASr. Regional Pharmacovigilance Officer
BayerThane, Maharashtra, INManager, Pharmacovigilance
ClarivateINDIASenior Data Specialist - Pharmacovigilance
YD Talent SolutionsNoida, Uttar Pradesh, IndiaImplementation Consultant Pharmacovigilance / Safety Systems
Veeva SystemsINDIASenior Pharmacovigilance Coordinator, Case Processing
ProPharma GroupIndiaPharmacovigilance,Medical Doctor
MEENAKSHI MISSION HOSPITAL AND RESEARCH CENTREINDIApharmacovigilance and medical coordinator
Randstad MENAINDIAPharmacovigilance Aggregate Reporting
Nityo Infotechundefined, IndiaPharmacovigilance Services Associate
myGworkBengaluru, India- Full-time
This job is with Accenture, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly.
Skill required : Pharmacovigilance Operations - Pharmacovigilance & Drug Safety Surveillance
Designation : Pharmacovigilance Services Associate
Qualifications : Any Graduation
Years of Experience : 1 to 3 years
Language - Ability : Japanese - Elementary
About Accenture
Accenture is a global professional services company with leading capabilities in digital, cloud and security.Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song— all powered by the world’s largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. We embrace the power of change to create value and shared success for our clients, people, shareholders, partners and communities.Visit us at www.accenture.com
What would you do? You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the world€™s leading biopharma companies bring their vision to life €" enabling them to improve outcomes by converging around the patient, connecting scientific expertise with unique insights into the patient experience.Management of the Affiliate Mailbox, reconciliation of reports per process, and performance of all written follow-up attempts to include both Serious and Non-serious cases.In this role, you will be expected to create and manage case identification, data entry, MedDRA coding, case processing, submission, and follow-ups for ICSRs in the safety database as per client guidelines and applicable global regulatory requirements.
What are we looking for?
- Agility for quick learning
- Collaboration and interpersonal skills
- Commitment to quality
- Ability to perform under pressure
- Prioritization of workload
Roles and Responsibilities :
Qualifications : Any Graduation