Pharmacovigilance Services New Associate

0-2 years

Not Disclosed

Bengaluru India

10 Feb. 18, 2025

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
Location: Bengaluru
Job No.: aioc-s01549672
Job Type: Full-time

Skill Required: Pharmacovigilance Services - Pharmacovigilance & Drug Safety Surveillance
Designation: Pharmacovigilance Services New Associate
Qualifications: Bachelor of Pharmacy
Years of Experience: 0 to 1 years
Language Ability: English - Advanced

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, 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. 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 in this vertical are part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory - helping the world’s leading biopharma companies bring their vision to life. This involves improving outcomes by converging around the patient, connecting scientific expertise with unique insights into the patient experience.

Key Responsibilities:

Manage the Affiliate Mailbox and perform reconciliation of reports per process.
Conduct all written follow-up attempts for both Serious and Non-serious cases.
Create and manage case identification, data entry, MedDRA coding, case processing, submission, and follow-ups for ICSRs in the safety database.
Ensure adherence to client guidelines and applicable global regulatory requirements.

What Are We Looking For?

Ability to solve routine problems, largely through precedent and general guidelines.
Primary interaction will be within your own team and direct supervisor.
Receive detailed instructions on all tasks.
Decisions made will impact your own work and will be closely supervised.
Individual contributor role within a team, with a predetermined, narrow scope of work.
Flexibility to work in rotational shifts may be required.

Qualifications:

Bachelor of Pharmacy (B.Pharm)
0 to 1 year of experience in pharmacovigilance or a related field.

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