Conducts economic analysis of pharmaceutical market dynamics and pricing. Develops pricing strategies for new product launches in Indian and global markets. Manages NPPA compliance and ceiling price calculations for DPCO products. Analyses tender pricing strategies for government and institutional business. Develops financial models for generic drug commercialization strategies. Conducts payer landscape analysis and supports market access strategies. Prepares commercial assessments for BD&L, licensing, and M&A transactions. Monitors competitor pricing, market share, and promotional spend data. Prepares economic inputs for product launch business plans. Coordinates with sales and marketing for revenue planning and forecasting. Supports policy advocacy with NPPA, NITI Aayog, and government bodies. Prepares market access dossiers for public procurement and PMBJP schemes. Stays updated with DPCO orders, NPPA policies, and pharmaceutical pricing trends.

Designs clinical databases and CRFs for Phase I to III clinical trials. Develops data management plans, data validation plans, and edit check specifications. Manages data entry, query management, and data cleaning across study sites. Conducts medical coding for adverse events and concomitant medications. Performs user acceptance testing for clinical database applications. Manages database lock activities and prepares data for statistical analysis. Ensures compliance with CDASH/CDISC standards for data collection and submission. Coordinates with CRO data management teams for outsourced trial operations. Prepares data management reports and presents to clinical project team. Maintains trial master file components related to data management activities. Ensures data integrity and audit trail compliance throughout the study. Supports regulatory inspections with data management documentation. Stays current with EDC platforms, CDISC updates, and data governance regulations.

Operates X-ray, CT, MRI, and fluoroscopy equipment for diagnostic imaging. Positions patients correctly to obtain high-quality diagnostic images. Ensures radiation safety and minimizes patient radiation exposure. Prepares patients for procedures including contrast-enhanced studies. Maintains imaging equipment and reports technical faults promptly. Follows AERB guidelines for radiation protection and safety. Ensures accurate patient identification and image labelling. Manages PACS image upload and archiving processes. Coordinates with radiologist for urgent and emergency studies. Maintains sterile technique for invasive radiology procedures. Prepares fluoroscopy and special procedure suites for radiologists. Documents all procedures and contrast administrations accurately. Trains student radiographers and new technologist inductees.

Position: Associate Clinical Research Associate - Oncology - NJ/NY An exceptional opportunity has arisen for a talented Associate Clinical Research Associate - Oncology - NJ/NY to contribute to our mission. The candidate will join a globally connected team that prizes diverse perspectives and operational excellence. Key Responsibilities: Maintain up-to-date knowledge of ICH E2A-E2F, GCP, and pharmacovigilance regulations. Ensure audit-readiness of safety documentation in line with GxP and regulatory expectations. Prepare high-quality clinical and regulatory documents aligned to CTD submission standards. Liaise with clinical, medical affairs, and regulatory teams for accurate safety data management. Ensure all cases are coded and processed per MedDRA and applicable global standards. Coordinate with CROs and licensing partners to fulfil pharmacovigilance obligations. Support collection and review of adverse event safety data from clinical and post-market sources. Contribute to risk management plans, SOPs, and signal detection and evaluation processes. Qualifications and Requirements: Minimum 35 years of progressive professional experience in a comparable role. High degree of professionalism, integrity, and alignment with organisational values. A bachelor's degree or higher in a relevant field; postgraduate qualifications are an added advantage. Proven ability to manage competing priorities in a deadline-driven, dynamic environment. Experience collaborating within cross-functional teams and matrix organisational structures. Strong analytical and problem-solving skills with the ability to navigate complex challenges. Knowledge of ICH E2A-E2F, MedDRA coding, GCP, and global regulatory requirements. This position represents a unique platform for a high-calibre professional to make a lasting contribution.

Position: TKI TA Head Oncology Global Pharmacovigilance We are seeking a highly qualified and motivated TKI TA Head Oncology Global Pharmacovigilance to join our dynamic and growing team. The selected professional will thrive in a data-driven, efficiency-focused, and collaborative work environment. Key Responsibilities: Conduct structured literature reviews and contribute to scientific summaries and labelling. Contribute to risk management plans, SOPs, and signal detection and evaluation processes. Coordinate with CROs and licensing partners to fulfil pharmacovigilance obligations. Support collection and review of adverse event safety data from clinical and post-market sources. Prepare high-quality clinical and regulatory documents aligned to CTD submission standards. Ensure audit-readiness of safety documentation in line with GxP and regulatory expectations. Ensure all cases are coded and processed per MedDRA and applicable global standards. Maintain up-to-date knowledge of ICH E2A-E2F, GCP, and pharmacovigilance regulations. Qualifications and Requirements: Proven ability to manage competing priorities in a deadline-driven, dynamic environment. High degree of professionalism, integrity, and alignment with organisational values. A bachelor's degree or higher in a relevant field; postgraduate qualifications are an added advantage. Experience collaborating within cross-functional teams and matrix organisational structures. Minimum 35 years of progressive professional experience in a comparable role. Strong analytical and problem-solving skills with the ability to navigate complex challenges. Knowledge of ICH E2A-E2F, MedDRA coding, GCP, and global regulatory requirements. We are committed to fostering an inclusive workplace and welcome applications from candidates of all backgrounds.