Pharmacovigilance Services Associate

1-3 years

Not Disclosed

Bengaluru

10 Dec. 26, 2024

Job Description

Job Type: Full Time Education: B.Sc./B.Pharm 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 Associate
Location: Accenture - Global Operations

About Accenture:
Accenture is a global professional services company with leading capabilities in digital, cloud, and security. We offer Strategy and Consulting, Technology and Operations services, and Accenture Song, powered by the world’s largest network of Advanced Technology and Intelligent Operations centers. With over 699,000 people serving clients in more than 120 countries, we leverage technology and human ingenuity to create value and shared success for all. Learn more at Accenture Careers.

Role Overview:
As a Pharmacovigilance Services Associate at Accenture, you will be part of our Life Sciences R&D vertical. You will work within the Pharmacovigilance & Drug Safety Surveillance team, responsible for managing Individual Case Safety Reports (ICSRs) in the safety database. You will support biopharma companies in maintaining drug safety compliance by handling case identification, data entry, MedDRA coding, and case processing. You will also perform follow-ups and submissions for both serious and non-serious adverse events as per global regulatory guidelines.

Key Responsibilities:

Case Management:
- Manage Affiliate Mailbox, reconciling reports per process and performing follow-up activities.
- Identify and enter cases accurately into the safety database, ensuring data integrity.
- Perform MedDRA coding and process ICSRs for serious and non-serious cases.
- Ensure timely case submission and follow-ups in alignment with client guidelines and regulatory requirements.
Regulatory Compliance:
- Adhere to global regulatory requirements for pharmacovigilance, ensuring compliance with all standards.
- Reconcile and manage reports in accordance with client specifications.
Problem-Solving & Execution:
- Solve routine problems through precedent and guidelines.
- Execute daily tasks with detailed instructions and follow-through on new assignments.
- Make decisions that impact your own work, with a focus on delivering quality results in the team setting.
Collaboration and Teamwork:
- Engage in daily interactions with your team and supervisor to meet the requirements of the role.
- As an individual contributor, follow a predetermined and focused scope of work within the team.
Shift Work:
- This role may require you to work in rotational shifts.

Qualifications and Experience:

Educational Background:
- BSc or Bachelor of Pharmacy.
Experience:
- 1 to 3 years of experience in Pharmacovigilance or Drug Safety surveillance.
Skills:
- Strong written and verbal communication skills.
- Adaptability and flexibility in a fast-paced environment.
- Ability to perform under pressure while maintaining accuracy in case processing.
- Knowledge of MedDRA coding and handling ICSRs.

Why Accenture?

Work with a global leader in Pharmacovigilance and Drug Safety.
Gain exposure to the biopharma industry and contribute to global regulatory compliance efforts.
Enjoy a dynamic work environment with opportunities for learning and career development.

Equal Opportunity Employment:
Accenture fosters an inclusive and diverse work environment, offering equal opportunities for all employees, including veterans and candidates with disabilities.

Apply Now to help shape the future of drug safety with Accenture!

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