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Pharmacovigilance Services Associate

0-3 years
Not Disclosed
10 Oct. 24, 2024
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

Skill Required: Pharmacovigilance Services - Pharmacovigilance & Drug Safety Surveillance
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. Combining unmatched experience and specialized skills across more than 40 industries, we offer 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 the entire life sciences enterprise, from research laboratories and clinical trials support to regulatory services and pharmacovigilance. Employees in this role will be part of one of the sub-offerings—Clinical, Pharmacovigilance & Regulatory—helping leading biopharma companies improve outcomes by connecting scientific expertise with unique insights into the patient experience.

Your responsibilities will include managing the Affiliate Mailbox, reconciling reports, and performing all written follow-up attempts for both Serious and Non-serious cases. You will be expected to create and manage case identification, data entry, MedDRA coding, case processing, submission, and follow-ups for Individual Case Safety Reports (ICSRs) in the safety database as per client guidelines and applicable global regulatory requirements.

What Are We Looking For?

  • Adaptable and flexible
  • Agility for quick learning
  • Commitment to quality
  • Ability to perform under pressure

Roles and Responsibilities

  • Solve routine problems, largely through precedent and referral to general guidelines.
  • Interact primarily within your team and with your direct supervisor.
  • Receive detailed to moderate instruction on daily work tasks and specific instruction on new assignments.
  • Make decisions that impact your own work.
  • Contribute individually as part of a team, focusing on a predetermined scope of work.
  • Please note that this role may require you to work in rotational shifts.