Drug Safety Analyst Job Title: Drug Safety Analyst Location(s): Pune, India About Springer Nature Springer Nature is one of the leading publishers of research in the world. We publish the largest number of journals and books and are a pioneer in open research. Through our leading brands, trusted for more than 180 years, we provide technology-enabled products, platforms and services that help researchers to uncover new ideas and share their discoveries, health professionals to stay at the forefront of medical science, and educators to advance learning. We are proud to be part of progress, working together with the communities we serve to share knowledge and bring greater understanding to the world. For more information, please visit about.springernature.com and follow @SpringerNature. About the Brand AdisInsight Safety provides tools to help pharma customers stay on top of their in-house pharmacovigilance (PV) literature monitoring. It provides comprehensive coverage of the literature for valid ICSRs and special situations across all drugs, collating information and data from global biomedical reference databases, in line with regulatory guidelines and industry best practice. AdisInsight Safety delivers comprehensive, high-quality safety intelligence by leveraging a cutting-edge, automated content acquisition process that blends advanced AI/ML technologies with expert human validation. This future-ready approach minimizes human error, ensures adaptability to evolving regulatory requirements, and enables the integration of diverse data sources. Users benefit from expanded access to safety-related content that is clearly categorized and easily filterable—making it simple to find the precise information needed for informed decision-making. About the Role The Drug Safety Analyst validates AI-generated safety content derived from biomedical literature as well as providing research, analysis and technical support for product development and continual improvement of Pharma Solutions safety products. The role is ideal for an established PV professional who wants to apply their skills and experience in a different setting, contributing to ongoing product quality and delivery as well as product development in the drug safety space, and continuing to help drive global patient safety. Role Responsibilities: Evaluates & validates AI-derived or published drug safety content in the regular and evolving production process, applying Scientific Comprehension and Pharmaceutical Industry Knowledge Conducts technical and domain research to create product & business value, identifying opportunities by linking domain & technical facts to broader business perspective through Customer Focus, Pharmaceutical Industry Knowledge and being Data Domain Savvy Communicates Effectively and Manages Complexity to clearly articulate product development issues and opportunities in discussions, presentations or documentation, keeping stakeholders focused on the key points. Contributes to Collaboration, shows Adaptability and Cultivates Innovation to enable continuous learning and improvement through shared reflection on processes and outcomes Drives Results by seeking new ways to optimize efficiency, quality and effectiveness Experience, Skills & Qualifications: Essential Masters or above in Pharmacy/LifeSciences/Medicine 3-5 years’ experience in PV or related drug safety discipline Candidates with significant experience in signal detection and management are preferred Strong understanding of PV workflows and fundamental principles of: Case processing, ICSR criteria and application to medical literature, MedDRA coding etc Signal identification and validation, disproportionality analysis, signal prioritization and evaluation, benefit-risk assessment and risk management Aggregate safety reporting Regulatory reporting requirements and compliance needs Logical & critical thinking, analytic skills, literature review capabilities Able to conduct technical domain research, identify issues, trends and opportunities Can link technical facts to broader perspectives (business, product, operations) and articulate implications and opportunities Strong English-language and scientific expression skills Able to conduct data/content checks with good attention to detail Self-motivation and enthusiasm with a collaborative attitude Ability to work independently with minimal/no supervision when needed #LI-SG2 Job Posting End Date: 5-10-2026
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- It is a Full Time Nurse / Compounder job for candidates with 3 - 5 years of experience.
More about this Drug Safety Analyst job
What qualifications and experience are required for this Drug Safety Analyst position?
Ans : Candidates should have All Education levels with 3-5 years of experience.
What is the salary and job type for this role?
Ans : Salary details will be shared during the hiring process.
What shift and timings does this job follow?
Ans : This Drug Safety Analyst job follows a Day shift.
Do you need to visit the office for this job?
Ans : Yes, candidates need to visit the office and work from the location in Baramati, Pune.
How many openings are available for this position?
Ans : There is 1 opening available for this position.
Is this job open for all genders?
Ans : Yes, this Drug Safety Analyst job is open for both male and female candidates.
Where is this job located?
Ans : This Drug Safety Analyst job is located in Baramati, Pune.
Why should you apply for this Drug Safety Analyst job?
Ans : The employer has not disclosed the salary for this role, but it is a Full Time opportunity with 1 opening available.