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Pharmacovigilance Services Analyst

3-4 years
Not Disclosed
10 Nov. 21, 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

Job Description: Pharmacovigilance Analyst

Skill Required: Pharmacovigilance Services - Pharmacovigilance & Drug Safety Surveillance
Designation: Analyst
Qualifications: Bachelor of Pharmacy
Years of Experience: 3 to 4 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, 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 across the entire life sciences enterprise, from research laboratories and clinical trials support, to regulatory services, pharmacovigilance, and patient services solutions. Employees in this vertical will be part of one of the sub-offerings—Clinical, Pharmacovigilance & Regulatory—helping the world’s leading biopharma companies bring their vision to life. You will enable them to improve outcomes by converging around the patient, connecting scientific expertise with unique insights into the patient experience.

Your role includes:

  • Managing the Affiliate Mailbox, reconciling reports per process, and performing written follow-up attempts for both Serious and Non-serious cases.
  • Creating and managing case identification, data entry, MedDRA coding, case processing, submission, and follow-ups for Individual Case Safety Reports (ICSRs) in the safety database, following client guidelines and applicable global regulatory requirements.

What Are We Looking For?

In this role, you will solve routine problems, primarily through precedent and referral to general guidelines. Your interactions will primarily be with your team and direct supervisor. You will receive detailed to moderate instructions on daily tasks and new assignments. Your decisions will impact your own work. You will be an individual contributor as part of a team with a predetermined, focused scope of work.

Please note that this role may require you to work in rotational shifts.

Roles and Responsibilities:

  • Solve routine problems using precedent and referral to guidelines.
  • Interact primarily with your team and direct supervisor.
  • Follow detailed instructions on daily tasks and new assignments.
  • Focus on a predetermined scope of work as an individual contributor.
  • Note: This role may require rotational shifts.