Instagram
youtube
Facebook

Pharmacovigilance Services Associate

0-3 years
Not Disclosed
10 Jan. 2, 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 Description: Pharmacovigilance Services Associate

Skill Required: Pharmacovigilance & Drug Safety Surveillance
Designation: Pharmacovigilance Services Associate
Qualifications: Bachelor of Pharmacy / Bachelor in Physiotherapy / BSc. Nursing
Years of Experience: 0 to 3 years

About Accenture
Accenture is a global professional services company with leading capabilities in digital, cloud, and security. We offer a wide range of services, including Strategy and Consulting, Technology and Operations, and Accenture Song, all powered by the world’s largest network of Advanced Technology and Intelligent Operations centers. With a global workforce of 699,000 people, we help clients across more than 120 countries achieve value and shared success through technology and human ingenuity. Learn more about us at www.accenture.com.

Role Overview
As part of our Life Sciences R&D vertical, you will contribute to a wide range of services across the life sciences enterprise. These services encompass everything from research laboratories, clinical trials support, and regulatory services to pharmacovigilance and patient services solutions. As a Pharmacovigilance Services Associate, you will support biopharma companies by enabling improved patient outcomes. This involves managing case identification, data entry, MedDRA coding, case processing, submission, and follow-ups for ICSRs (Individual Case Safety Reports) in the safety database, in alignment with client guidelines and global regulatory standards.

Key Responsibilities:

  • Case Management: Manage affiliate mailbox and reconcile reports according to prescribed processes.
  • Data Entry and Processing: Perform all written follow-ups and case processing for both Serious and Non-serious cases, ensuring timely and accurate reporting.
  • MedDRA Coding: Handle MedDRA coding and case submission in the safety database as per regulatory requirements.
  • Teamwork & Collaboration: Work closely with your team and supervisor to complete tasks, solve routine problems, and contribute to team goals.
  • Continuous Learning: Stay agile and adaptable, with a focus on quickly learning and applying new knowledge.
  • Shift Work: Please note that this role may involve working in rotational shifts.

Skills and Qualities We Are Looking For:

  • Ability to perform under pressure and deliver results
  • Strong teamwork skills and adaptability
  • Quick learning ability and flexibility in handling new challenges
  • Ability to work within established guidelines and processes
  • Strong communication skills and attention to detail

What You’ll Need to Succeed:

  • Ability to follow detailed instructions and apply guidelines effectively
  • Basic decision-making impacting individual work
  • Ability to interact and collaborate within the team and with your supervisor

Join Accenture to work in a dynamic environment that blends human expertise and cutting-edge technology to help improve patient outcomes and advance the life sciences industry.