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Pharmacovigilance Services Associate

Freshers years
3 LPA to 5 LPA
15 July 19, 2024
Job Description
Job Type: Full Time Education: BSC, MSC, B Pharma, M Pharma, Pharma D Skills: Causality Assessment, Communication Skills, GCP guidelines, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, Medical Terminology, Narrative Writing, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Pharmacovigilance Services Associate

Location: Chennai

Job Number: AIOC-S01535310

Employment Type: Full-Time

 

Note: At any given point in time, you can only have one "Active" application.

 

Job Description

Skill Required:

  • Pharmacovigilance Services - Pharmacovigilance & Drug Safety Surveillance

Designation:

  • Pharmacovigilance Services Associate

Qualifications:

  • Bachelor of Pharmacy

  • Bachelor of Physiotherapy

  • BSc. Nursing

Years of Experience:

  • Freshers

Language Ability:

  • English - Intermediate

 

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.

 

Job Responsibilities

Overview:

You will be aligned with our Life Sciences R&D vertical. Our services span the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the world’s leading biopharma companies bring their vision to life, enabling them to improve outcomes by converging around the patient, connecting scientific expertise with unique insights into the patient experience.

Key Responsibilities:

  • Management of the Affiliate Mailbox

  • Reconciliation of reports per process

  • Performance of all written follow-up attempts for both Serious and Non-serious cases

  • Create and manage case identification, data entry, MedDRA coding, case processing, submission, and follow-ups for ICSRs in the safety database as per client guidelines and applicable global regulatory requirements

What We Are Looking For

  • Ability to perform under pressure

  • Collaboration and interpersonal skills

  • Prioritization of workload

  • Commitment to quality

Roles and Responsibilities

  • Solve routine problems, largely through precedent and referral to general guidelines

  • Interact primarily within your own team and direct supervisor

  • Receive detailed to moderate level of instruction on daily work tasks and detailed instruction on new assignments

  • Decisions made will impact your own work

  • Be an individual contributor as a part of a team, with a predetermined, focused scope of work

  • Note: This role may require you to work in rotational shifts