Conducts primary and secondary market research for pharmaceutical business planning. Designs and manages physician surveys, patient insight studies, and advisory panels. Analyses IMS Health and IQVIA data for market size and share assessments. Prepares competitive landscape analysis and brand positioning reports. Conducts demand forecasting and market sizing for new products. Analyses prescription audit data and prepares therapy area market reports. Monitors competitor product launches, pricing changes, and promotional activities. Prepares market entry analysis for new geographies and therapy areas. Coordinates with marketing and sales teams to provide market intelligence. Manages market research vendor relationships and project budgets. Prepares presentation-ready insights and recommendations for senior management. Supports business development with market opportunity analysis reports. Stays current with pharma market research methodologies and real-world data tools.

Manages financial planning, budgeting, and forecasting for the pharma business. Prepares monthly, quarterly, and annual financial statements and MIS reports. Manages accounts payable, accounts receivable, and cash flow operations. Ensures compliance with GST, income tax, and other statutory requirements. Manages cost accounting for pharmaceutical manufacturing operations. Coordinates internal and statutory audits and ensures timely closure. Prepares financial analysis to support business decisions and investments. Manages relationships with banks, financial institutions, and auditors. Ensures transfer pricing compliance for international business transactions. Prepares financial due diligence reports for BD and licensing transactions. Manages ERP-based financial module and data integrity in financial systems. Supports costing for new products and pricing decisions for sales team. Stays current with Ind AS, IFRS convergence, and pharmaceutical sector tax policies.

Manages hospital information systems, EHR, and digital health infrastructure. Oversees HMIS, LIS, PACS, and RIS system implementation and operations. Manages IT team responsible for hardware, software, and network support. Ensures 24/7 availability of critical hospital IT systems and applications. Develops IT strategy aligned with hospital digital transformation goals. Manages IT security, access controls, and data backup protocols. Implements and manages telemedicine and digital health platforms. Ensures compliance with data privacy and healthcare IT regulations. Manages vendor relationships for IT services and system contracts. Supports NABH and JCI digital health documentation requirements. Prepares IT budgets and manages capital and operational expenditures. Conducts IT risk assessments and business continuity planning. Trains staff on new IT systems and digital health tools.

Evaluates and treats disorders of the brain, spine, and nervous system. Diagnoses epilepsy, stroke, Parkinson's disease, and multiple sclerosis. Performs and interprets EEG, nerve conduction studies, and EMG. Manages acute stroke protocols including thrombolysis decisions. Conducts lumbar punctures and interprets CSF analysis results. Collaborates with neurosurgeons on operative case planning. Manages patients in neurology ICU and step-down units. Prescribes and monitors complex neurological medications. Counsels patients and families on neurological conditions. Supervises neurology residents and conducts case presentations. Participates in neurological MDT discussions for complex cases. Stays updated with international neurology guidelines and trials. Contributes to research and publishes in peer-reviewed journals.

Position: Clinical Data Manager We are on the lookout for a well-rounded Clinical Data Manager to contribute to our operational and strategic priorities. The organisation is committed to nurturing talent and providing a platform for exceptional career growth. Duties and Accountabilities: ? Ensure audit-readiness of safety documentation in line with GxP and regulatory expectations. ? Review and analyse PSURs, PBRERs, DSURs, and other aggregate safety reports. ? Ensure all cases are coded and processed per MedDRA and applicable global standards. ? Support collection and review of adverse event safety data from clinical and post-market sources. ? Maintain up-to-date knowledge of ICH E2A-E2F, GCP, and pharmacovigilance regulations. ? Prepare high-quality clinical and regulatory documents aligned to CTD submission standards. ? Assist in preparing and submitting regulatory safety reports in compliance with ICH guidelines. ? Liaise with clinical, medical affairs, and regulatory teams for accurate safety data management. Key Skills and Qualifications: ? Commitment to professional ethics, confidentiality, and the highest standards of conduct. ? Sound understanding of organisational dynamics and stakeholder management in complex environments. ? Advanced competency in analytical tools, reporting platforms, and role-specific technology. ? Effective presentation skills with the ability to communicate complex ideas with clarity. ? Leadership experience with a track record of guiding teams, projects, or cross-functional initiatives. ? 5+ years of experience with demonstrated progression in scope, complexity, and responsibility. ? Knowledge of ICH E2A-E2F, MedDRA coding, GCP, and global regulatory requirements. A competitive compensation structure along with performance incentives and growth opportunities awaits the right candidate.