Manages government affairs and policy advocacy for pharmaceutical company. Builds relationships with Ministry of Health, CDSCO, NPPA, and NITI Aayog officials. Monitors drug policy developments and prepares impact assessments for the business. Represents company at industry associations including IDMA, OPPI, and PharmExcil. Prepares position papers, policy briefs, and submissions to government consultations. Manages corporate social responsibility programs in health and community areas. Coordinates media and public relations activities for the pharmaceutical company. Supports DPCO compliance and manages interactions with NPPA on pricing matters. Develops external affairs strategy for new drug launches and regulatory advocacy. Manages relationships with patient advocacy groups and civil society organizations. Prepares briefing documents for senior management meetings with government officials. Coordinates with legal team on legislative and regulatory compliance monitoring. Stays current with pharmaceutical industry policy developments and global health agenda.

Develops and implements environment, health, and safety management systems. Ensures compliance with Factories Act, environmental laws, and EHS regulations. Manages hazardous chemical handling, storage, and disposal procedures. Conducts workplace risk assessments and implements risk mitigation measures. Manages industrial effluent treatment plant (ETP) and pollution control operations. Leads safety incident investigation and root cause analysis programs. Prepares and submits environmental compliance reports to SPCB and CPCB. Manages occupational health programs including medical surveillance and hygiene. Conducts fire safety, hazmat, and emergency response training and drills. Manages contractor safety programs and work permit systems at plant. Prepares EHS performance metrics and reports for management reviews. Supports EHS due diligence for new plant acquisitions or expansions. Stays current with environmental regulations, GreenCo standards, and safety codes.

Coordinates and manages telemedicine consultation services for patients. Schedules and manages virtual OPD appointments across specialties. Trains doctors and patients on telemedicine platform usage. Ensures smooth video consultation experiences and technical support. Manages patient records, prescriptions, and digital documentation. Coordinates with pharmacy for digital prescription fulfilment. Monitors telemedicine adoption metrics and patient satisfaction scores. Resolves technical issues and escalates to IT team as needed. Ensures compliance with telemedicine guidelines issued by NMC and MoHFW. Builds referral networks with primary care providers for teleconsultations. Prepares weekly telemedicine utilization and performance reports. Coordinates follow-up consultations and specialist referrals. Manages telemedicine platform vendor relationships and improvements.

Diagnoses and manages malignant tumors across multiple cancer types. Designs individualized chemotherapy and targeted therapy protocols. Coordinates multidisciplinary tumor board discussions for patient cases. Administers and monitors systemic anti-cancer treatments. Manages chemotherapy side effects and supportive oncology care. Interprets PET-CT, biopsy, and molecular diagnostic reports. Counsels patients on treatment options, prognosis, and palliative care. Participates in clinical trials and cancer research programs. Collaborates with radiation and surgical oncology teams. Monitors treatment response using RECIST and other criteria. Provides survivorship care and long-term follow-up plans. Stays current with NCCN, ESMO, and ASCO guidelines. Mentors oncology fellows and trains junior medical staff.

Position: Clinical Data Manager Our organisation invites applications from accomplished professionals for the role of Clinical Data Manager. This role sits within a fast-paced, innovation-driven organisation that values integrity and continuous improvement. Primary Duties and Responsibilities: Plan, monitor, and close clinical trials in compliance with GCP and ICH guidelines. Conduct benefit-risk assessments and contribute to clinical development strategy discussions. Provide clinical site training on data collection standards and regulatory requirements. Review source data and ensure completeness, accuracy, 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. Monitor safety signals and liaise with pharmacovigilance teams for adverse event management. Prepare and maintain essential trial documents including protocols, ICFs, and CSRs. Required Qualifications: At least 24 years of hands-on experience in a comparable professional setting. Exceptional organisational skills with the ability to handle multiple concurrent responsibilities. Strong interpersonal and stakeholder management skills with a client-service orientation. Bachelor's degree in a relevant discipline; master's degree or professional certification is preferred. Detail-oriented mindset with the ability to synthesise and present complex information clearly. Proficiency in relevant software and digital tools specific to the functional area. 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.