PV Literature Surveillance Expert at Sanofi Consumer Healthcare
Location: Hyderabad
Job Type: Full-Time
Application Deadline: December 20, 2024
About Sanofi Consumer Healthcare
Sanofi Consumer Healthcare is a global leader in healthcare, committed to empowering individuals with innovative health solutions. Our focus is on sustainability, social responsibility, and improving everyday health and well-being.
Job Overview
Sanofi Consumer Healthcare is hiring a PV Literature Surveillance Expert to manage and maintain literature surveillance processes related to adverse event reporting. The role involves developing search strategies for retrieving scientific and medical literature, performing quality checks, and ensuring compliance with pharmacovigilance (PV) regulations.
Key Responsibilities
- Search Strategy Development:
- Design and maintain search strategies for retrieving relevant scientific and medical literature.
- Literature Review:
- Review literature records and identify valid cases for database entry.
- Conduct quality checks on search strategies to ensure accuracy and compliance.
- Local Journal Management:
- Identify and manage local journals critical for literature search operations.
- Stakeholder Interaction:
- Collaborate with internal and external stakeholders to resolve literature search-related issues.
- Data Entry & Maintenance:
- Enter validated adverse event cases into relevant databases.
- Assess literature references for validity and request full articles as necessary.
- Quality Assurance:
- Conduct product reference checks and maintain trackers for compliance and reporting.
- Regulatory Reporting:
- Prepare bibliographic outputs for regulatory reports and submissions.
Required Qualifications
| Qualification | Details |
|---|---|
| Education | M.Sc. / M.Pharm / Life Sciences |
| Experience | Minimum 3 years in biomedical literature review, specifically for adverse event reporting |
| Location | Hyderabad |
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Required Skills
- Scientific Knowledge:
Strong understanding of medical literature and pharmacovigilance processes. - Regulatory Compliance:
Familiar with pharmacovigilance regulations, adverse event reporting, and drug safety systems. - Writing Proficiency:
Ability to prepare and review scientific and regulatory documents effectively.
Key Competencies
- Attention to Detail:
Ability to critically assess literature and identify relevant adverse event cases. - Analytical Skills:
Strong problem-solving abilities and decision-making capabilities. - Communication:
Excellent verbal and written communication skills for interacting with stakeholders and preparing regulatory reports. - Time Management:
Efficient in handling multiple tasks and meeting deadlines.
Why Join Sanofi?
Sanofi offers a dynamic work environment focused on innovation and continuous learning. As a PV Literature Surveillance Expert, you’ll play a key role in ensuring drug safety and contributing to global healthcare.
How to Apply
Interested candidates can apply online. Ensure that your application is submitted before December 20, 2024.