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Bengaluru, Karnataka, India
Hybrid
GCL : F
Introduction to role:
Are you ready to set the clinical safety strategy that safeguards patients while accelerating transformative medicines? This role puts you at the center of benefit-risk decisions for high-impact therapies, guiding products from development through post-marketing with clarity, speed and scientific rigor.
You will lead the safety strategy for assigned programs, translating sophisticated data into crucial actions that shape labeling, risk minimization and regulatory outcomes. Working across functions and geographies, you will align guides around a clear safety narrative and ensure that patient protection and business objectives move forward together. How will you use your clinical judgement and leadership to anticipate risk, advise pivotal decisions and help bring life-changing treatments to patients faster?
Safety Strategy and Governance: Own the clinical safety strategy for assigned products across late-stage development and post-marketing, including defining identified and potential risks, proposing mitigation and minimization measures, setting safety go/no-go criteria, and shaping the risk component of benefit-risk assessments at project and governance forums.
Risk Management Planning: Review and endorse core Patient Risk Management Plans and provide medical expertise to safety specifications, pharmacovigilance plans and risk minimization activities across core, development and locally reviewed plans; ensure risk minimization strategies are implemented in product reference safety information.
Clinical Development Integration: Provide strategic clinical safety input to development planning; give to project-specific safety requirements; review and approve investigator brochures, protocols, informed consents and study reports; engage with external data supervising committees as appropriate.
Signal Detection and Evaluation: Lead or give to surveillance activities including medical review of individual cases, signal detection and evaluation; identify and use appropriate data sources; collaborate with external providers; deliver clear, fit-for-purpose safety evaluations and chip in to SIRC activities and collaborator discussions, including with Patient Safety leadership and QPPV/Deputy QPPV.
Labeling and Regulatory Interactions: Provide medical input to labeling updates and responses to regulatory requests, including strategic input for local label deviations; in consultation with PS scientists and clinical teams, prepare Developmental Core Safety Information for development products.
Regulatory Reports and Submissions: Provide medical input and review of periodic reports (PBRERs, PSURs, DSURs) and renewal documentation; lead Patient Safety contributions to global submissions (NDA, BLA, MAA) for products, formulations or indications.
Cross-Functional Leadership: Represent Patient Safety on clinical and project teams; facilitate Safety Management or Safety Review Teams; give to ad hoc teams addressing urgent safety issues; present safety information at investigator and commercial meetings as needed.
External Engagement and Governance: Give to PS components of Safety Agreements; advise on licensing agreements; participate in external meetings with regulators, partners and opinion leaders; support due diligence and, when appropriate, product liability litigation.
Quality, Audit and Improvement: Maintain inspection readiness; raise issues promptly and appropriately; lead or participate in process improvement initiatives; propose methodological and process innovations; mentor and train junior team members in signal evaluation, risk management and safety reporting.
Collaboration and Culture: Work seamlessly with preclinical safety, informatics, safety science and other guides to ensure robust evaluation of safety data; understand and support the pharmacovigilance system and the role of the QPPV; collaborate effectively across functions, cultures and external providers.
When we put unexpected teams in the same room, we unleash ambitious thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.
Join a scientific community where industry and academia meet to accelerate discovery, and where a diverse set of minds align around an unusual purpose: improving outcomes for patients. You will work with unexpected teams in the same room fueling ambitious thinking, backed by sophisticated technology and a rich pipeline spanning multiple indications. We partner widely, from hundreds of preclinical collaborations across many countries to a coalition of leading cancer centers, to address some of the toughest diseases. Here, your judgement and curiosity are encouraged, your voice matters, and your impact reaches patients globally; we value kindness alongside ambition and provide the support to grow while pursuing breakthroughs that change lives.
If you are ready to lead safety strategy that protects patients and builds breakthrough medicines, take the next step and share your application to make your impact felt now.
Date Posted
05-Oct-2026Closing Date
22-Oct-2026AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.
