Pharmacovigilance Services Sr Analyst

Accenture; Chennai District; On-site; INR 1,200,000 - 1,800,000; Full time

Job summary

Accenture is seeking a Pharmacovigilance Services Sr Analyst in Chennai, India. The role requires a Bachelor of Pharmacy and 5–8 years of experience in pharmacovigilance, with emphasis on safety writing and medical referencing. Proficiency in MS Office and strong communication skills are expected.

The candidate will develop high-quality medical content, support regulatory submissions, manage affiliate reports, and mentor junior writers in a dynamic team environment.

Qualifications

• Primary skill in pharmacovigilance safety writing and medical writing.

Responsibilities

• Develop high-quality medical scientific content outlines and guide the team for content development in line with client expectations.
• Manage affiliate mailbox reconciliation, report follow-ups, and MLR review-related queries.
• Develop narrative summaries of adverse events for regulatory submissions and safety reports.
• Collaborate with cross-functional teams to support MLR review processes and implement required changes.
• Train and mentor scientific writers and ensure quality delivery and client engagement.

Skills

Safety Writing

Education

Bachelor of Pharmacy

Job description

Skill required:

Pharmacovigilance Operations - Safety Writing

Designation:

Pharmacovigilance Services Sr Analyst

Qualifications:

Bachelor of Pharmacy

Years of Experience:

5 to 8 years

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 784,000 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?

• Use scientific expertise to develop high-quality medical scientific content outlines and guide the team in content development for assigned modules projects in line with client expectations.
• Management of the Affiliate Mailbox reconciliation of reports per process and performance of all written follow up attempts to include both Serious and Non serious cases
• Manage and develop individual case narratives describing adverse events for inclusion in regulatory submissions and safety reports for completed interim clinical study reports.

What are we looking for?

• Primary skill - Safety Writing - P5
• Bachelor s or Master s degree in pharmacy life sciences.
• 5 - 8 years of relevant experience in reviewing medical documents Medical referencing.
• Proficiency in medical referencing techniques and awareness of industry standards.
• Exhibit proficiency in MS Office applications, including Excel, Adobe Acrobat, Outlook, and PowerPoint.
• Strong organizational skills and attention to detail.
• Effective interpersonal and communication skills.
• Ability to work well in a dynamic team environment.
• Experience with Veeva Vault PromoMats Vault ProMotion is

Roles and Responsibilities

• Use scientific expertise to develop high-quality medical scientific content outlines and guide the team in content development for assigned modules projects in line with client expectations.
• Collaborate with cross-functional teams to support the medical legal regulatory (MLR) review process, respond to MLR review committee queries, and implement required changes effectively.
• Experience in writing white papers, manuscripts, point of view, etc.
• Write scientific content for projects if the nature of the project is extremely complex and it requires expertise or based on business need.
• Communicate the clinical data in a clear and concise manner.
• Follow department best practices for processes, communication, project management, documentation, and technical requirements.
• Converts relevant data and information into a form that meets regional regulatory requirements.
• Understands and complies with appropriate conventions and other governing bodies following applicable divisional guidelines, templates, and SOPs to comply with regulatory requirements.
• Completes assignments independently or for more complex documents, under the guidance of a mentor.
• Ensure compliance with client and Accenture internal SOPs for all materials.
• Collaborate with technology and creative teams to develop innovative digital solutions.
• Train and mentor scientific writers, contributing to s
• Use scientific expertise to develop high-quality medical scientific content outlines and guide the team in content development for assigned modules projects in line with client expectations.
• Collaborate with cross-functional teams to support the medical legal regulatory (MLR) review process, respond to MLR review committee queries, and implement required changes effectively.
• Experience in writing white papers, manuscripts, point okill development.
• Ensure quality delivery and client engagement for organic growth.

Bachelor of Pharmacy

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