Develops and drives corporate strategy for the pharmaceutical company. Leads long-term strategic planning and portfolio prioritization decisions. Manages M&A pipeline including identification, evaluation, and integration planning. Conducts strategic market analysis and competitive intelligence programs. Develops therapy area strategy and portfolio diversification recommendations. Leads business planning process and connects strategy to annual operating plans. Manages relationships with investment banks, PE firms, and strategic advisors. Represents strategy function at board meetings and investor presentations. Leads international market expansion strategy and new territory assessments. Manages strategic projects and cross-functional transformation programs. Develops partnership and alliance strategies for growth acceleration. Evaluates disruptive trends including digital health, biosimilars, and specialty pharma. Stays current with global pharma strategy, healthcare economics, and industry disruption.

Leads pharmacovigilance operations for marketed products and clinical programs. Manages a team of PV specialists and ensures quality of safety case processing. Oversees ICSR management, aggregate report preparation, and signal detection. Ensures compliance with global PV regulations including EU, US, and CDSCO. Maintains and updates pharmacovigilance system master file (PSMF). Manages safety data exchange agreements with global partners and licensees. Leads preparation and submission of PSURs, PBRERs, and DSURs to authorities. Coordinates with regulatory affairs for labeling updates based on safety data. Represents PV function in regulatory authority inspections and audits. Manages risk minimization activities and risk management plan implementation. Provides pharmacovigilance training to medical, marketing, and field teams. Develops SOPs and quality systems for the pharmacovigilance function. Stays updated with EMA, FDA, ICH E2A-F guidelines, and PV regulations globally.

Conducts health economic analyses including cost-effectiveness modelling. Develops budget impact models for payer and hospital decision-making. Reviews and synthesizes real-world evidence and clinical trial data. Prepares health technology assessment (HTA) submissions. Collaborates with medical affairs on value dossier development. Conducts quality-of-life and PRO (patient-reported outcome) research. Analyzes epidemiological and health service utilization data. Supports market access teams with economic evidence for reimbursement. Presents HEOR data at scientific conferences and advisory boards. Publishes health economic research in peer-reviewed journals. Develops budget impact tools for key account management teams. Trains internal teams on health economic concepts and models. Monitors HTA decisions and reimbursement landscape globally.

Diagnoses and treats musculoskeletal disorders, fractures, and injuries. Performs joint replacement, arthroscopy, and fracture fixation surgeries. Manages spine conditions including disc disease and deformity correction. Conducts pre and post-operative orthopaedic patient assessments. Interprets X-rays, MRI, and CT scans for orthopaedic diagnosis. Collaborates with physiotherapists on rehabilitation protocols. Handles emergency trauma cases and polytrauma management. Performs sports injury surgeries and ligament reconstruction. Supervises orthopaedic residents and scrub staff in theatre. Participates in bone and joint MDT discussions. Manages paediatric orthopaedic conditions and congenital deformities. Stays updated with orthopaedic implant technologies and techniques. Contributes to orthopaedic research and clinical publications.

Position: Clinical Data Manager We are looking for a strategic and detail-oriented Clinical Data Manager to deliver excellence across key functions. The incumbent will operate in a structured yet agile environment that prioritises quality and professional growth. Duties and Accountabilities: Support collection and review of adverse event safety data from clinical and post-market sources. Participate in regulatory inspections, health authority meetings, and internal audits. Ensure all cases are coded and processed per MedDRA and applicable global standards. Review and analyse PSURs, PBRERs, DSURs, and other aggregate safety reports. Conduct structured literature reviews and contribute to scientific summaries and labelling. Ensure audit-readiness of safety documentation in line with GxP and regulatory expectations. Contribute to risk management plans, SOPs, and signal detection and evaluation processes. Maintain up-to-date knowledge of ICH E2A-E2F, GCP, and pharmacovigilance regulations. Key Skills and Qualifications: Leadership experience with a track record of guiding teams, projects, or cross-functional initiatives. Advanced competency in analytical tools, reporting platforms, and role-specific technology. Commitment to professional ethics, confidentiality, and the highest standards of conduct. Critical and strategic thinking skills with the ability to translate insights into clear actions. Recognised qualification in the relevant professional field at the undergraduate or graduate level. Sound understanding of organisational dynamics and stakeholder management in complex environments. Knowledge of ICH E2A-E2F, MedDRA coding, GCP, and global regulatory requirements. This is an outstanding opportunity for a motivated professional to advance their career within a reputable organisation.