Provides occupational health services to employees at pharmaceutical manufacturing sites. Conducts pre-employment, periodic, and exit medical examinations for all workers. Manages occupational disease surveillance programs for chemical and solvent exposure. Provides first aid, emergency medical care, and coordinates hospital referrals. Develops and implements medical surveillance programs for hazardous chemical handlers. Reviews Material Safety Data Sheets and provides health risk communication to workers. Manages respiratory protection and biological exposure monitoring programs. Conducts health promotion programs including nutrition, fitness, and wellness. Prepares health records, maintains registers as required under Factories Act. Coordinates with EHS team on chemical hygiene, ergonomics, and safety programs. Investigates occupational illnesses and prepares health impact assessments. Provides medical clearance for specific jobs including cleanroom and chemical handling. Stays current with OSHA regulations, NIOSH guidelines, and occupational medicine practice.

Manages clinical trial operations across multiple study sites and protocols. Leads a team of CRAs and ensures site monitoring quality and compliance. Reviews monitoring visit reports and escalates critical findings appropriately. Manages CRO relationships and oversees third-party clinical operations. Develops site management plans, monitoring plans, and risk-based monitoring strategies. Coordinates with data management and biostatistics teams for data review. Ensures timely submission of clinical study reports and regulatory filings. Manages study budgets, site payments, and milestone tracking systems. Leads inspection readiness programs for regulatory authority audits. Prepares and delivers training for CRAs on protocols and GCP compliance. Manages trial master file completeness and archival for completed studies. Supports business development by reviewing clinical feasibility for new studies. Stays current with adaptive trial designs, CDSCO regulations, and GCP updates.

Assigns accurate ICD-10, CPT, and HCPCS codes to patient diagnoses and procedures. Reviews medical records, physician notes, and clinical documentation for coding. Ensures coding accuracy for insurance billing and revenue cycle management. Audits coded records for errors and compliance with payer guidelines. Collaborates with physicians on clinical documentation improvement. Stays updated with annual ICD and CPT code changes and updates. Manages coding productivity targets and accuracy quality metrics. Handles coding queries from billing and insurance teams. Participates in coding audits and external compliance reviews. Supports denial management by reviewing and correcting coding errors. Maintains knowledge of DRG grouping and case mix management. Trains junior coders and documentation specialists. Prepares monthly coding accuracy and productivity reports.

Position: Clinical Supply Chain Manager (CAM) We invite a proactive and capable Clinical Supply Chain Manager (CAM) to lead and execute within a collaborative, agile environment. The organisation fosters a culture of continuous learning, development, and shared organisational accountability. Duties and Accountabilities: Conduct structured literature reviews and contribute to scientific summaries and labelling. Coordinate with CROs and licensing partners to fulfil pharmacovigilance obligations. Contribute to risk management plans, SOPs, and signal detection and evaluation processes. Ensure audit-readiness of safety documentation in line with GxP and regulatory expectations. Maintain up-to-date knowledge of ICH E2A-E2F, GCP, and pharmacovigilance regulations. Support collection and review of adverse event safety data from clinical and post-market sources. 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. Advanced competency in analytical tools, reporting platforms, and role-specific technology. Leadership experience with a track record of guiding teams, projects, or cross-functional initiatives. Sound understanding of organisational dynamics and stakeholder management in complex environments. Effective presentation skills with the ability to communicate complex ideas with clarity. 5+ years of experience with demonstrated progression in scope, complexity, and responsibility. Knowledge of ICH E2A-E2F, MedDRA coding, GCP, and global regulatory requirements. Successful candidates will receive access to ongoing professional development and industry-leading resources.

Position: Clinical Data Manager An exciting career opportunity exists for a motivated Clinical Data Manager to advance their professional journey. This role sits within a fast-paced, innovation-driven organisation that values integrity and continuous improvement. Principal Responsibilities: Review source data and ensure completeness, accuracy, and regulatory compliance. Prepare and maintain essential trial documents including protocols, ICFs, and CSRs. Manage medical coding using MedDRA and WHO Drug Dictionary for clinical trial data. Monitor safety signals and liaise with pharmacovigilance teams for adverse event management. Provide clinical site training on data collection standards and regulatory requirements. 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. Plan, monitor, and close clinical trials in compliance with GCP and ICH guidelines. Candidate Requirements: Sound understanding of organisational dynamics and stakeholder management in complex environments. 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. Critical and strategic thinking skills with the ability to translate insights into clear actions. Commitment to professional ethics, confidentiality, and the highest standards of conduct. Recognised qualification in the relevant professional field at the undergraduate or graduate level. Knowledge of ICH E2A-E2F, MedDRA coding, GCP, and global regulatory requirements. The organisation provides a comprehensive benefits package and excellent career advancement opportunities for the right candidate.