Develops patient access programs and affordability schemes for pharmaceutical products. Manages government tender, PMBJP, and public health procurement strategies. Builds relationships with government health departments, NITI Aayog, and payers. Develops reimbursement dossiers and value dossiers for insurance coverage. Manages compassionate use, named patient programs, and early access schemes. Monitors insurance coverage decisions and manages formulary inclusion activities. Coordinates with medical affairs on health economics and outcomes evidence. Develops strategic access plans for rare disease and specialty products. Prepares policy advocacy documents for drug pricing and access reform. Coordinates with state health departments for drug supply under NHM programs. Analyzes patient journey data to identify access barriers and develop solutions. Manages NGO and patient advocacy group relationships for therapy areas. Stays updated with PM-JAY coverage policies, NPPA regulations, and health schemes.

Manages end-to-end supply chain operations for pharmaceutical products. Develops demand forecasting models using historical data and market trends. Coordinates with manufacturing, procurement, and logistics teams for supply. Manages inventory levels across warehouses, depots, and C&F agents. Ensures product availability at stockists to prevent stockouts and shortages. Manages cold chain logistics for temperature-sensitive pharmaceutical products. Coordinates import and export activities for API, excipients, and finished goods. Implements S&OP (Sales and Operations Planning) processes for the business. Tracks supply chain KPIs including fill rate, OTIF, and inventory turns. Manages ERP system data integrity and supply chain module configurations. Develops contingency plans for supply disruptions and raw material shortages. Ensures compliance with GDP guidelines for pharmaceutical product distribution. Stays current with pharma supply chain regulations, serialization, and track-and-trace.

Conducts drug discovery and formulation research for new pharmaceutical products. Synthesizes and evaluates new chemical entities for therapeutic activity. Performs in-vitro and in-vivo pharmacological screening studies. Develops and optimizes drug formulations for target delivery systems. Conducts stability studies and stress testing of pharmaceutical products. Analyzes drug-excipient compatibility and physicochemical properties. Prepares scientific reports and contributes to regulatory dossiers. Manages laboratory notebooks, data integrity, and documentation standards. Collaborates with analytical, clinical, and regulatory teams. Operates analytical equipment including HPLC, GC, and spectrophotometers. Stays updated with IP landscape and files patents for novel discoveries. Participates in scientific conferences and publishes research findings. Mentors junior scientists and graduate research interns.

Position: Bioinformatics Analyst We are currently recruiting a results-oriented Bioinformatics Analyst to strengthen our high-performing team. This is an excellent opportunity for professionals who value structured career advancement and meaningful impact. Primary Duties and Responsibilities: Prepare and maintain essential trial documents including protocols, ICFs, and CSRs. Conduct benefit-risk assessments and contribute to clinical development strategy discussions. Maintain trial master files and ensure ongoing audit-readiness and regulatory compliance. Develop SOPs, work instructions, and training materials for clinical operations teams. Track milestones and coordinate with sites, CROs, and sponsors for on-time delivery. Review source data and ensure completeness, accuracy, and regulatory compliance. Monitor safety signals and liaise with pharmacovigilance teams for adverse event management. Manage medical coding using MedDRA and WHO Drug Dictionary for clinical trial data. Required Qualifications: Bachelor's degree in a relevant discipline; master's degree or professional certification is preferred. Proficiency in relevant software and digital tools specific to the functional area. Exceptional organisational skills with the ability to handle multiple concurrent responsibilities. At least 24 years of hands-on experience in a comparable professional setting. Strong interpersonal and stakeholder management skills with a client-service orientation. Commitment to ongoing professional learning and industry knowledge enhancement. Knowledge of ICH E2A-E2F, MedDRA coding, GCP, and global regulatory requirements. We look forward to welcoming a driven professional who shares our commitment to excellence and sustained impact.

Position: Senior Manager, Health Economics & Outcomes Research (HEOR) Our organisation invites applications from accomplished professionals for the role of Senior Manager, Health Economics & Outcomes Research (HEOR). This position is embedded within a high-functioning team that prizes collaboration, innovation, and quality. Main Accountabilities: Review source data and ensure completeness, accuracy, and regulatory compliance. Track milestones and coordinate with sites, CROs, and sponsors for on-time delivery. Support IND, NDA, MAA, and dossier submissions with high-quality regulatory documentation. Develop SAS programs for SDTM/ADaM dataset creation and table, figure, listing generation. Monitor safety signals and liaise with pharmacovigilance teams for adverse event management. Prepare and maintain essential trial documents including protocols, ICFs, and CSRs. Manage medical coding using MedDRA and WHO Drug Dictionary for clinical trial data. Conduct benefit-risk assessments and contribute to clinical development strategy discussions. Essential Skills and Experience: 4+ years of experience with a demonstrated track record of growth and professional impact. Collaborative, proactive, and able to operate effectively with minimal supervision. Knowledge of applicable regulatory frameworks, industry standards, and compliance requirements. Superior writing and communication skills with experience preparing executive-level documents. Relevant undergraduate or postgraduate degree aligned with the role's core responsibilities. Strong project management capabilities with experience in agile or structured methodologies. Knowledge of ICH E2A-E2F, MedDRA coding, GCP, and global regulatory requirements. Applications are reviewed on a rolling basis; suitably qualified individuals are encouraged to apply promptly.