Medical Advisor, Ideation & Portfolio Development
Dr Reddys
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Job summary
Dr Reddys is seeking a Medical Advisor Ideation and Portfolio Development to lead scientific evaluation and differentiation of new product opportunities across therapeutic areas. You will work closely with Portfolio, R&D, Clinical Development, Regulatory and other cross-functional teams to assess scientific literature, clinical data and treatment guidelines for India-focused portfolio decisions.
The role covers ideation through to product selection, development and readiness for launch, ensuring
Qualifications
- MBBS with MD pharmacology or postgraduate qualification in a relevant medical discipline.
- 2–5 years in pharma with Medical Affairs, portfolio evaluation or clinical development.
- Experience in scientific evaluation of pipeline assets is advantageous.
Responsibilities
- Lead scientific evaluation of pipeline opportunities with cross-functional teams.
- Provide medical recommendations for Go/No-Go product selection decisions.
- Collaborate with Portfolio, R&D, Clinical Development and Regulatory teams.
- Support product differentiation through clinical and scientific rationale.
- Translate data into portfolio development decisions and strategic insights.
- Assist in regulatory and launch readiness with medical input.
Skills
Education
Job description
MBBS with M.D. Pharmacology/Medicine or full-time postgraduate qualification in an appropriate medical discipline.
2-5 years of relevant pharmaceutical industry experience in Medical Affairs, Portfolio Evaluation, Clinical Development, R&D interface, New Product Planning or related roles.
Experience in scientific evaluation of pipeline assets, new product ideation, product differentiation or cross-functional drug development would be an advantage.
The Medical Advisor Ideation & Portfolio Development will provide scientific and clinical leadership for the identification, evaluation, differentiation and development of new product opportunities across therapeutic areas.
The role will work closely with Portfolio, R&D, Clinical Development, Regulatory and other cross-functional teams to evaluate pipeline opportunities through comprehensive assessment of scientific literature, clinical evidence, treatment guidelines, competitive intelligence, global development pipelines and relevant medical/scientific databases.
The Medical Advisor will contribute across the end-to-end product journeyfrom ideation and opportunity evaluation through product selection, development, regulatory approval and readiness for launch, following which the product is transitioned to the respective Medical Affairs/Commercial teams.
- Continuously evaluate the global pharmaceutical and clinical development landscape to identify potential new product, molecule, indication, formulation and combination opportunities.
- Conduct structured searches across scientific literature, clinical trial registries, regulatory databases, treatment guidelines, competitive intelligence platforms and other relevant databases.
- Identify emerging mechanisms of action, evolving standards of care, unmet medical needs and therapeutic areas with potential relevance to the India portfolio.
- Generate scientifically differentiated product concepts based on clinical need, emerging evidence and competitive landscape.
- Lead comprehensive medical evaluation of pipeline opportunities in collaboration with the Portfolio team.
- Assess opportunities based on:
- Unmet medical need and current standard of care
- Target patient population and patient journey
- Mechanism of action and biological rationale
- Clinical efficacy and safety
- Comparative clinical positioning
- Global and Indian treatment guidelines
- Development stage and probability of clinical success
- Competitive and future treatment landscape
- Potential differentiation in the Indian market
- Develop clear medical recommendations and scientific rationale for Go/No-Go product selection decisions.
- Present medical evaluations and recommendations to cross-functional teams and relevant governance/decision-making forums.
- Work closely with the Portfolio/Business Development teams to scientifically assess internal and external product opportunities.
- Provide the medical perspective for prioritisation and selection of differentiated portfolio opportunities.
- Support assessment of molecules, combinations, formulations, indications and lifecycle opportunities proposed for portfolio inclusion.
- Translate complex scientific and clinical evidence into clear strategic recommendations for portfolio decision-making.
- Partner closely with R&D/Formulation Development teams to identify opportunities for meaningful product differentiation.
- Provide medical input into the development of:
- Novel formulations
- Fixed-dose combinations
- Dose/strength optimisation
- Drug-delivery approaches
- New indications
- Patient-centric product features
- Define the clinical and medical rationale for differentiation versus currently available standards of care and anticipated future competitors.
- Ensure proposed differentiation addresses a meaningful physician, patient or healthcare-system need rather than being purely formulation-driven.
- Provide medical and scientific inputs throughout the drug/product development process.
- Contribute to development strategy, target product profile and clinical development considerations wherever required.
- Provide inputs into study concepts, endpoints, patient populations, comparators and other clinically relevant aspects of development.
- Review and interpret emerging clinical data and assess its implications for the evolving product strategy.
- Collaborate with Clinical Development, R&D and Regulatory teams to address scientific or clinical questions arising during development.
- Provide medical inputs for regulatory strategy and submissions for new products/indications.
- Support scientific responses to regulatory queries and participate in regulatory/subject expert discussions wherever required.
- Ensure that the scientific positioning of the product remains aligned with available evidence and the proposed clinical use throughout the approval process.
- Develop a clear medical product narrative covering unmet need, target patient, clinical value proposition, differentiation and appropriate positioning.
- Support medical readiness during the pre-launch phase.
- Once the product reaches the appropriate stage of approval/launch readiness, ensure structured handover of scientific strategy, evidence and product positioning to the respective Medical Affairs and launch teams.
- Provide scientific support during transition to ensure continuity from the original product concept to its intended clinical positioning.
The role will work extensively with:
- Strong scientific and clinical evaluation capabilities
- Ability to critically interpret clinical trials and medical literature
- Understanding of drug development and regulatory pathways
- Strong understanding of treatment guidelines and evolving standards of care
- Ability to assess unmet need, clinical differentiation and future competitive landscapes
- Strong analytical and strategic thinking
- Ability to integrate information from multiple scientific databases and sources into actionable recommendations
- Ability to translate science into portfolio and product-development decisions
- Intellectual curiosity and strong external/pipeline orientation
- Effective cross-functional collaboration in a matrix environment
- Strong written, presentation and stakeholder-management skills
- Ability to manage multiple therapeutic areas and product evaluations simultaneously
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