Accenture Pharmacovigilance vacancies Chennai: Senior Medical Review Scientist

Are you a seasoned Medical Review Scientist looking for a stimulating opportunity in the heart of Chennai? Accenture invites passionate individuals to join our vibrant team as Senior Medical Review Scientists. Dive into the dynamic world of pharmacovigilance and contribute to groundbreaking advancements in life sciences research. Discover more about our company and the exciting vacancies available below.

About Accenture

Founded on the principles of innovation and excellence, Accenture stands as a global leader in professional services. With a focus on digital transformation, cloud solutions, and security, we empower clients across 40+ industries to thrive in an ever-evolving landscape. Our team of over 699,000 professionals operates from the world’s largest network of Advanced Technology and Intelligent Operations centers, serving clients in 120+ countries. At Accenture, we embrace change as a catalyst for value creation and shared success.

Accenture Chennai Vacancies List

Explore the following opportunities to join our esteemed team in Chennai:

Position Title: Senior Medical Review Scientist
Company Name: Accenture
Salary: Competitive, commensurate with experience
Detailed Job Description: Refer to the section below for a comprehensive overview.

Senior Medical Review Scientist Vacancies in Chennai at Accenture

Job Description

Role:

Senior Medical Review Scientists play a pivotal role within our Life Sciences R&D vertical, contributing to various aspects of pharmacovigilance and patient services solutions.

Industry Type:

Pharmaceuticals / Clinical Research

Department:

Pharmacovigilance

Employment Type:

Full-time

Role Category:

R&D / Life Sciences

Educational Background Required:

MBBS
Additional qualifications in pharmacovigilance preferred

Key Skills:

Medical Review, Pharmacovigilance, Clinical Documentation, Regulatory Compliance, Team Management

Responsibilities

As a Senior Medical Review Scientist at Accenture, your responsibilities include:

Conducting clinical review of medical records to ensure compliance with Medicare standards.
Assessing the seriousness, causality, and labeling of adverse events in accordance with client SOPs and global regulatory requirements.
Collaborating with stakeholders to resolve disputes and manage multiple projects under pressure.
Authoring and reviewing various clinical documents, including protocols, investigator brochures, and safety narratives.

How to Apply

Ready to embark on an enriching career journey with Accenture? Apply now