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Pharmacovigilance Services Associate

1-3 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 Services Associate

Skill Required: Pharmacovigilance Services - Pharmacovigilance & Drug Safety Surveillance
Designation: Pharmacovigilance Services Associate
Qualifications: Bachelor of Pharmacy
Years of Experience: 1 to 3 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, clinical trials support, and regulatory services to pharmacovigilance and patient services solutions. Employees in this area will be part of one of the sub-offerings—Clinical, Pharmacovigilance & Regulatory—helping the world’s leading biopharma companies bring their vision to life by improving outcomes, converging around the patient, and connecting scientific expertise with unique insights into the patient experience.

In this role, you will manage the Affiliate Mailbox, reconcile reports per process, and perform written follow-ups for both serious and non-serious cases. You will be responsible for case identification, data entry, MedDRA coding, case processing, submission, and follow-ups for ICSRs in the safety database according to client guidelines and global regulatory requirements.

What Are We Looking For?

In this role, you will be solving routine problems, mainly based on precedent and referral to general guidelines. Your expected interactions will be with your own team and direct supervisor. You will receive detailed instructions on daily tasks and moderate guidance on new assignments. The decisions you make will impact your own work, and you will contribute as an individual to 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 based on precedent and general guidelines.
  • Interact with your team and direct supervisor on a daily basis.
  • Receive detailed instructions on daily tasks and moderate guidance for new assignments.
  • Your decisions will primarily impact your own work.
  • As an individual contributor, you will work within a focused scope of responsibilities.
  • Note: This role may require you to work in rotational shifts.