Accenture Hiring Pharmacovigilance Services Associate in Chennai

Accenture Hiring Pharmacovigilance Services Associate in chennai

Accenture Hiring Pharmacovigilance Services Associate: Join Team in Chennai

Accenture, a global leader in professional services, is currently seeking qualified individuals to join their Life Sciences R&D vertical as Pharmacovigilance Services Associates in Bengaluru. This is a full-time opportunity designed for professionals passionate about drug safety and pharmacovigilance. If you hold a Master of Pharmacy degree and possess 1 to 3 years of experience in Pharmacovigilance & Drug Safety Surveillance, this role could be your gateway to a rewarding career at Accenture.

About Accenture

Accenture is a globally recognized professional services company known for its expertise in digital, cloud, and security services. With specialized skills across over 40 industries, Accenture offers 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. With a workforce of 699,000 employees, Accenture serves clients in more than 120 countries, driving innovation and excellence in every project.

Job Role: Pharmacovigilance Services Associate

As a Pharmacovigilance Services Associate at Accenture, you will be aligned with the Life Sciences R&D vertical, providing essential services across the life sciences enterprise. Your role will involve working with clinical trials, regulatory services, and pharmacovigilance solutions to help leading biopharma companies achieve their goals. Specifically, you will focus on the management of the Affiliate Mailbox, report reconciliation, and the follow-up of both Serious and Non-serious cases. Your responsibilities will include case identification, data entry, MedDRA coding, case processing, submission, and follow-ups for Individual Case Safety Reports (ICSRs) in compliance with client guidelines and global regulatory requirements.

Key Responsibilities

• 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.
• You will be part of a dynamic Pharmacovigilance team with array of capabilities ranging from detection, assessment, understanding and prevention of adverse effects or any other medicine/vaccine related problem following Good Pharmacovigilance Practice (GVP) per client SOPs and applicable global regulatory requirements (Individual Case Safety Reports) to working on various aspects of Aggregate reports such as planning, authoring, reviewing and publishing of PBRER, PSUR, DSUR, PADER, Addendum to clinical overview (AdCO), Risk Management Plan (RMP), Signal detection and validation reports (SDVR), Cosmetovigilance Safety Reports (CoSR).
• The Pharmacovigilance team is also responsible for authoring and reviewing clinical documents such Protocols and amendment, Investigator Brochure, Clinical Study Reports (CSR), Synoptic/Abbreviated CSR, Safety Narratives, Clinical O In this role, you will be expected to manage and develop individual case narratives describing adverse events for inclusion in regulatory submissions and safety reports for completed/interim clinical study reports.

Qualifications and Experience

To be considered for this role, candidates must have:

• Skill required: Pharmacovigilance Services – Pharmacovigilance & Drug Safety Surveillance
• Designation: Associate
• Qualifications:Bachelor of Pharmacy
• Years of Experience:1 – 3 Years

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Tagged as: Global Pharma Jobs, Good Clinical Practice (GCP)