- Location
- Telangana (Sandoz), India
- Type
- Full-time
- Department
- Healthcare
- Seniority
- Senior
- Experience
- 8+ years
- Closing date
- Today
- Source
- Workday
Description
Job Description Summary
Responsible for delivery of Early Program Biosimilar Pipeline Support within the Medical Affairs Operations organization based out of GCC India. The role ensures high-quality analytical, scientific, and medical writing support, delivers insight-driven outputs aligned to business and program needs, and partners with Global Medical Affairs and cross-functional stakeholders to ensure operational delivery and continuous improvement across Early Program biosimilar support services.Job Description
Responsible for delivery of Early Program Biosimilar Pipeline Support within the Medical Affairs Operations organization based out of GCC India. The role ensures high-quality analytical, scientific, and medical writing support, delivers insight-driven outputs aligned to business and program needs, and partners with Global Medical Affairs and cross-functional stakeholders to ensure operational delivery and continuous improvement across Early Program biosimilar support services.
Your Key Responsibilities:
Your responsibilities include, but not limited to:
Own delivery of higher-complexity medical writing, analytical, desk research, and competitive intelligence support in line with defined project objectives and quality expectations.
Generate scientific and strategic insights through analysis and synthesis of data, evidence, competitive intelligence, and relevant external information.
Create and manage fit-for-purpose outputs such as molecule overviews, insight summaries, therapeutic area / product landscape summaries, and slide-based materials.
Manage delivery across diverse medical and scientific topics, adapting effectively to evolving priorities, timelines, and stakeholder requests.
Engage proactively with Global Medical Affairs, Early Program teams, and other relevant stakeholders to ensure timely, aligned, and high-quality delivery of outputs.
Apply appropriate analytical platforms, databases, and AI-enabled tools responsibly to gather, analyze, and synthesize information, as applicable. Ensure full adherence to confidentiality requirements and documentation expectations when handling proprietary or pipeline-related information.
Implement knowledge sharing, alignment with related support teams, and continuous improvement of ways of working across the Early Program support stream.
Support the transition and stabilization of services into GCC and contribute to process standardization, documentation, and operational maturity.
What you’ll bring to the role:
Essential Requirements:
Early Program analytical and writing outputs are delivered effectively and in line with defined quality, timeliness, and stakeholder expectations. Scientific and strategic insights are accurate, well synthesized, and translated into fit-for-purpose deliverables.
Stakeholder alignment, coordination, and delivery visibility are maintained effectively across the support model.
Confidentiality, documentation quality, and process expectations are consistently maintained.
Identified risks / gaps are addressed in a timely manner, with appropriate remediation and continuous improvement actions.
Education: Advanced degree or equivalent qualification in life science, healthcare, pharmacy, medicine, or related field preferred with 8–12+ years experience in the pharmaceutical / healthcare industry, ideally with experience in medical writing, analytical support, competitive intelligence, scientific communications, and/or related Medical Affairs support models.
Subject matter expertise in scientific / medical analysis, desk research, competitive intelligence, insight synthesis, and slide-based communication.
Experience working across diverse medical and scientific domains, ideally including biosimilars, oncology, immunology, or related therapeutic areas. Artificial Intelligence savy, including high awareness of its limitations. Aware of specific confidentiality requirements of pipeline work and experience working in a cross-functional and global environment.
You’ll receive:
Breakdown of benefits received in this role. Include flexible working, learning and development opportunities as well.
Why Sandoz?
Sandoz is the global leader in Biosimilar and Generic medicines, a segment of the healthcare industry that delivers 80% of the world’s medicines at 30% of the cost, touching the lives of more than 1 billion people across 100+ countries! While we are proud of our achievements, we have an ambition to do more so that everyone can achieve the basic human right of good health.
With investments in new development capabilities, production sites, new acquisitions, and partnerships, we have the opportunity to shape the future of Sandoz and help even more people gain access to low-cost, high-quality medicines, sustainably.
Our momentum is powered by an open, collaborative culture driven by our talented and ambitious colleagues, who, in return for applying their skills, experience an agile and collegiate environment with impactful careers, where diversity of thought is welcomed and where personal growth is supported!
Join us, help us make healthcare fairer and faster.
Commitment to Diversity & Inclusion:
We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
Skills Desired
Building Construction, Clinical Practices, Clinical Research, Clinical Trials, Drug Development, Hazard Identification, Health Sciences, Immunology, Intensive Care UnIT (Icu), Internal Control, Internal Medicine, Job Description, Medical Information, Organization Skills, Patient Care, Stakeholder Engagement, Tcp/Ip Protocols, Utilization Management (Um)Skills
Clinical TrialsPatient Care
