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Pharmacovigilance Services New Associate

Accenture
Accenture
0-2 years
Not Disclosed
Bengaluru, India
10 March 9, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Pharmacovigilance Services New Associate
Company: Accenture
Location: Bengaluru, India
Job Type: Full-Time
Experience Required: 0–2 Years
Job ID: AIOC-S01630317

About Accenture
Accenture is a leading global professional services company specializing in digital, cloud, and security solutions. With extensive experience across more than 40 industries, Accenture delivers services in Strategy and Consulting, Technology, and Operations. The company is supported by a global network of Advanced Technology and Intelligent Operations Centers and a workforce of over 784,000 professionals serving clients in more than 120 countries. Accenture combines technology and human ingenuity to help organizations innovate, transform, and create sustainable value for clients, partners, shareholders, and communities.

Role Overview
Accenture is seeking a Pharmacovigilance Services New Associate to join its Life Sciences R&D vertical in Bengaluru. This role is ideal for entry-level professionals interested in drug safety, pharmacovigilance operations, and regulatory compliance within the pharmaceutical and biotechnology industry. The selected candidate will support pharmacovigilance processes that ensure the safety and effectiveness of pharmaceutical products throughout their lifecycle.

Key Responsibilities

  • Perform case identification and data entry related to Individual Case Safety Reports (ICSRs) in the pharmacovigilance safety database.

  • Conduct MedDRA coding and support case processing activities according to client guidelines and global regulatory standards.

  • Assist in the preparation and submission of safety reports to regulatory authorities.

  • Monitor and follow up on pharmacovigilance cases to ensure completeness and regulatory compliance.

  • Analyze safety data collected from clinical trials, healthcare professionals, and patient reports.

  • Collaborate with internal teams to ensure timely processing of drug safety information.

  • Follow standard operating procedures (SOPs) and global pharmacovigilance guidelines.

Required Qualifications

  • Master of Science (MSc) in Life Sciences or related field

  • Bachelor of Pharmacy (B.Pharm)

  • Master of Pharmacy (M.Pharm)

Experience Requirements

  • 0 to 2 years of experience in pharmacovigilance, drug safety, or related life sciences roles.

  • Fresh graduates with relevant academic knowledge in pharmacovigilance and drug safety are encouraged to apply.

Skills and Competencies

  • Basic understanding of pharmacovigilance operations and drug safety surveillance.

  • Familiarity with global regulatory requirements related to adverse event reporting.

  • Knowledge of MedDRA coding and ICSR case processing is an advantage.

  • Strong analytical and attention-to-detail skills.

  • Effective communication and teamwork abilities.

Work Environment

  • This position requires close collaboration with team members and supervisors.

  • Tasks will be performed according to detailed instructions and established guidelines.

  • The role involves handling routine pharmacovigilance processes under supervision.

  • Candidates should be comfortable working in rotational shifts if required.

Why Join Accenture
Working at Accenture provides an opportunity to contribute to global life sciences and healthcare innovation. Employees gain exposure to leading pharmaceutical and biotechnology organizations while developing expertise in pharmacovigilance, regulatory operations, and patient safety initiatives.

Location
Bengaluru, India.