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Pharmacovigilance Services New Associate

0-1 years
Not Disclosed
10 Oct. 8, 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

Skill Required: Pharmacovigilance Services - Pharmacovigilance & Drug Safety Surveillance
Designation: Pharmacovigilance Services New Associate
Qualifications: BSc
Years of Experience: 0 to 1 year
Language Proficiency: English - Proficient

Accenture is a global professional services company with leading capabilities in digital, cloud, and security. With unmatched experience and specialized skills across more than 40 industries, 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. Our 699,000 employees 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.

In this role, you will be aligned with our Life Sciences R&D vertical, contributing to various aspects of the life sciences enterprise—from research laboratories to clinical trials support and regulatory services, including pharmacovigilance and patient services solutions. As part of our Clinical, Pharmacovigilance & Regulatory sub-offering, you will help leading biopharma companies bring their vision to life by improving outcomes through a patient-centered approach.

Responsibilities:

  • Manage the Affiliate Mailbox and reconcile reports as per process.
  • Perform written follow-ups for both Serious and Non-serious cases.
  • Create and manage case identification, data entry, MedDRA coding, case processing, submissions, and follow-ups for Individual Case Safety Reports (ICSRs) in the safety database, adhering to client guidelines and applicable global regulatory requirements.

What Are We Looking For?

  • Adaptable and flexible
  • Ability to perform under pressure
  • Strong teamwork skills
  • Commitment to quality
  • Effective written and verbal communication

Additional Details:

  • This role involves solving routine problems, largely following established guidelines and precedents.
  • You will receive detailed instructions on all tasks, with decisions impacting your own work closely supervised.
  • This position requires individual contribution as part of a team with a narrow scope of work.
  • Please note that this role may require you to work in rotational shifts.