Accenture Hiring Pharmacovigilance – Safety Writing Professionals

Accenture Hiring Pharmacovigilance - Safety Writing Professionals
  • Full Time
  • bangalore

Accenture Hiring Pharmacovigilance – Safety Writing Professionals

Are you a seasoned Pharmacovigilance professional looking for an exciting career opportunity? Look no further! Accenture is on the lookout for skilled individuals to join their dynamic team. Read on to explore the captivating world of Pharmacovigilance at Accenture.

About the Company (Accenture)

Accenture is a global professional services company renowned for its expertise in digital, cloud, and security solutions. With a workforce of 699,000 professionals across 40 industries, Accenture is committed to delivering cutting-edge technology and intelligent operations. The company’s services span Strategy and Consulting, Technology and Operations, and Accenture Song—powered by the world’s largest network of Advanced Technology and Intelligent Operations centers. Visit Accenture to discover more.

Company Vacancies List

Position Title Company Name
Senior Regulatory Services Scientist Accenture in India

Job Description

About the Department & Responsibilities

Join Accenture’s Life Sciences R&D vertical, where services cover the entire life sciences spectrum, including research, clinical trial support, regulatory services, pharmacovigilance, and patient services solutions. As a Senior Regulatory Services Scientist, you will:

  1. Support Public Disclosure: Ensure public disclosure of Clinical Study Reports (CSRs), statistical documents, synopsis, protocols, and other clinical documents adhering to client and regulatory requirements.
  2. Privacy Protection: Redact clinical documents to protect the privacy of individuals, groups, and staff associated with a clinical study.
  3. Quality Review: Conduct quality reviews of redacted clinical documents following specific guidelines.
  4. Timely Finalization: Complete redaction and incorporate quality control (QC) comments within agreed timelines.
  5. Training and Compliance: Provide training to new team members and ensure compliance with EU Policy 70 and Health Canada guidelines on clinical data transparency.
  6. Narrative Writing: Handle Clinical Submission Narrative Writing for Phase 1-4 clinical trials as a Project Lead.

Educational Background Required

  • Qualifications: Bachelor of Pharmacy
  • Experience: 7 to 11 years

How to Apply

Interested candidates can apply for this exciting opportunity by Clicking below link

Apply online

Accenture Hiring Pharmacovigilance - Safety Writing Professionals
Accenture Hiring Pharmacovigilance – Safety Writing Professionals

To apply for this job please visit www.accenture.com.


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