Clinical Research Physician

Role & Responsibilities
• Drive clinical development activities across assigned products and programs
• Collaborate with internal teams and external stakeholders including CROs and investigators
• Oversee safety reporting, medical review, and clinical documentation
• Contribute to medical writing, scientific communications, and clinical study reports
• Ensure audit and inspection readiness across clinical development activities
• Support project management, timelines, and cross-functional coordination
• Ensure strict adherence to regulatory, compliance, and ethical guidelines

Qualification
• MD with 5–10 years of relevant clinical research or pharmaceutical experience
• OR DM Clinical Pharmacology with 1–2 years of experience in pharma, biotech, or CRO clinical development

Experience
• Proven experience in pharmaceutical industry clinical development processes
• Exposure to regulatory strategy and product lifecycle management
• Experience working with CROs, regulatory bodies, and internal development teams

Skills
• Strong understanding of clinical research and drug development processes
• Expertise in safety reporting and medical review
• Medical writing and scientific documentation skills
• Knowledge of regulatory compliance and inspection readiness
• Strong communication, coordination, and project management abilities

About the Company
• Troikaa Pharmaceutical Ltd. is a research-led pharmaceutical organisation, Specialises in Novel Drug Delivery Systems (NDDS), Focused on innovation, compliance, and high-quality clinical development.