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Pharmacovigilance Services New Associate

0-1 years
Not Disclosed
10 Oct. 7, 2024
Job Description
Job Type: Full Time Remote 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

Position: Pharmacovigilance Services New Associate
Skill Required: Pharmacovigilance & Drug Safety Surveillance
Qualifications: Bachelor of Pharmacy / Bachelor of Physiotherapy / BSc in Nursing
Experience: 0 to 1 year


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, employees, shareholders, partners, and communities. Visit us at www.accenture.com.


What You Will 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 trial support to regulatory services, pharmacovigilance, and patient services solutions. In this role, you will be part of the Clinical, Pharmacovigilance & Regulatory sub-offering, helping leading biopharma companies bring their vision to life by improving outcomes through a patient-centric approach.

Your responsibilities will include managing the Affiliate Mailbox, reconciling reports as per process, and performing all written follow-up attempts for both Serious and Non-serious cases. You will also 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 according to client guidelines and applicable global regulatory requirements.


What We Are Looking For

  • Ability to perform under pressure
  • Strong teamwork skills
  • Adaptability and flexibility
  • Quick learning agility

Roles and Responsibilities

  • Solve routine problems primarily through reference to general guidelines and established precedents.
  • Interact mainly within your team and with your direct supervisor.
  • Follow detailed instructions for all tasks assigned.
  • Make decisions that impact your work, under close supervision.
  • Work as an individual contributor within a team with a predetermined, narrow scope of responsibilities.
  • Be prepared to work in rotational shifts as required.