Develops primary and secondary packaging solutions for pharmaceutical products. Conducts compatibility studies for drug-container closure system interactions. Evaluates packaging materials including blister foils, HDPE bottles, and vials. Designs and executes packaging stability studies per ICH Q1 guidelines. Coordinates with regulatory affairs for packaging-related regulatory submissions. Manages packaging artwork development and approval process. Conducts equipment trials for new packaging lines and packaging formats. Manages packaging specification development and change control processes. Supports cost optimization initiatives for packaging materials and designs. Coordinates with procurement for packaging material qualification and sourcing. Prepares packaging development reports and contributes to dossier sections. Ensures compliance with BIS, Pharmacopoeial, and international packaging standards. Stays updated with sustainable packaging trends, child-resistant, and tamper-evident requirements.

Manages a team of medical representatives across an assigned territory. Sets individual and team sales targets aligned with regional business goals. Conducts regular field visits to coach and mentor medical representatives. Analyses sales data to identify gaps, opportunities, and growth areas. Builds relationships with key opinion leaders (KOLs) and senior physicians. Plans and executes product launch strategies in the assigned territory. Monitors competitor activity and develops counter-strategies for the team. Reviews daily call reports and sales performance dashboards regularly. Organizes CME programs, roundtable meetings, and doctor engagement events. Manages stockist networks and resolves supply chain issues in the territory. Prepares monthly sales forecasts and submits reports to regional management. Recruits, trains, and onboards new medical representatives as needed. Ensures compliance with company promotional guidelines and ethical standards.

Diagnoses and treats mental health disorders across diverse patient populations. Manages depression, schizophrenia, bipolar disorder, and anxiety disorders. Prescribes and monitors psychotropic medications with regular review. Performs psychiatric evaluations and risk assessments for patients. Provides psychotherapy and evidence-based therapeutic interventions. Manages inpatient psychiatric unit and crisis stabilization. Collaborates with psychologists, social workers, and counsellors. Handles medico-legal cases and forensic psychiatric evaluations. Participates in addiction medicine and de-addiction programs. Supervises psychiatric residents and mental health staff. Conducts outpatient and community mental health programs. Contributes to mental health awareness and stigma reduction. Stays current with DSM-5, ICD-11, and psychiatric research.

Position: Clinical Data Manager Our organisation is looking for an ambitious Clinical Data Manager committed to quality outcomes and sustained growth. This is an opportunity to be part of a purpose-driven team reshaping industry standards and best practices. Key Deliverables and Responsibilities: Monitor safety signals and liaise with pharmacovigilance teams for adverse event management. Conduct benefit-risk assessments and contribute to clinical development strategy discussions. Develop SOPs, work instructions, and training materials for clinical operations teams. Maintain trial master files and ensure ongoing audit-readiness and regulatory compliance. Plan, monitor, and close clinical trials in compliance with GCP and ICH guidelines. Develop SAS programs for SDTM/ADaM dataset creation and table, figure, listing generation. Provide clinical site training on data collection standards and regulatory requirements. Manage medical coding using MedDRA and WHO Drug Dictionary for clinical trial data. Professional Requirements: Hands-on experience with tools, software, and platforms standard to the profession. Familiarity with regulatory, compliance, or quality frameworks applicable to the industry. A structured, results-driven approach with the ability to meet defined milestones consistently. Strong communication, presentation, and interpersonal skills across all organisational levels. Willingness to travel, adapt, and take on additional responsibilities as the business demands. 26 years of relevant industry experience with evidence of increasing responsibility. Knowledge of ICH E2A-E2F, MedDRA coding, GCP, and global regulatory requirements. We value talent and invest in our people this role offers both professional challenge and meaningful rewards.

Position: Clinical Data Manager An exceptional opportunity has arisen for a talented Clinical Data Manager to contribute to our mission. The selected professional will thrive in a data-driven, efficiency-focused, and collaborative work environment. Scope of Responsibilities: Conduct structured literature reviews and contribute to scientific summaries and labelling. Ensure all cases are coded and processed per MedDRA and applicable global standards. Assist in preparing and submitting regulatory safety reports in compliance with ICH guidelines. Ensure audit-readiness of safety documentation in line with GxP and regulatory expectations. Liaise with clinical, medical affairs, and regulatory teams for accurate safety data management. 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. Coordinate with CROs and licensing partners to fulfil pharmacovigilance obligations. Competencies and Qualifications: Ability to work both independently and in a team-oriented, collaborative environment. Bachelor's degree in a relevant discipline; master's degree or professional certification is preferred. Exceptional organisational skills with the ability to handle multiple concurrent responsibilities. Detail-oriented mindset with the ability to synthesise and present complex information clearly. Strong interpersonal and stakeholder management skills with a client-service orientation. Commitment to ongoing professional learning and industry knowledge enhancement. 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.