Clinical Research Physicians

Why This Role Matters
Clinical Research Physicians play a critical role in advancing innovative drug development programs. In a research-led organization specializing in Novel Drug Delivery Systems (NDDS), this position ensures scientific rigor, regulatory compliance, patient safety oversight, and effective clinical development strategy execution.

Job Description
Troikaa Pharmaceutical Ltd. is seeking a Clinical Research Physician with strong clinical development expertise. The selected candidate will collaborate with internal and external stakeholders to drive clinical programs, ensure safety monitoring, maintain inspection readiness, and support medical documentation and regulatory compliance across development projects.

Key Features of the Role:
• Research-led pharmaceutical organization
• Focus on Novel Drug Delivery Systems (NDDS)
• Strategic role in clinical development lifecycle
• Exposure to regulatory strategy and compliance
• Cross-functional collaboration with global stakeholders

Responsibilities
• Drive clinical development activities across product lifecycle
• Capture and review safety reports and clinical data
• Contribute to medical writing and scientific communications
• Ensure documentation accuracy and audit/inspection readiness
• Collaborate with regulatory, pharmacovigilance, and operations teams
• Support project management for clinical programs
• Ensure strict adherence to compliance and ethical guidelines
• Participate in regulatory strategy and lifecycle management discussions

Required Qualifications
• MD with 5–10 years of relevant experience
OR
• DM in Clinical Pharmacology with 1–2 years of pharmaceutical/biotech/CRO clinical development experience

Educational Requirements:
• MD (mandatory)
• DM Clinical Pharmacology (acceptable alternative pathway)

Experience and Skills:
• Experience in pharmaceutical clinical development processes
• Understanding of regulatory strategy and lifecycle management
• Strong safety reporting and documentation skills
• Experience in medical writing and scientific communication
• Knowledge of audit and inspection readiness standards
• Excellent stakeholder management and collaboration skills
• Strong understanding of compliance and ethical frameworks

Age Eligibility:
As per company norms

Salary Insights
Compensation details not disclosed. Industry-standard remuneration aligned with senior clinical development roles.

Company Overview
Troikaa Pharmaceuticals Ltd. is a research-driven pharmaceutical company with expertise in Novel Drug Delivery Systems (NDDS). The organization focuses on innovative formulations and robust clinical development strategies to deliver differentiated therapeutic solutions while maintaining high compliance and ethical standards.

FAQs

Is prior pharmaceutical industry experience required?
Yes, relevant clinical development experience in pharma/biotech/CRO is required.

Is DM Clinical Pharmacology eligible?
Yes, DM Clinical Pharmacology with relevant industry exposure is eligible.

Does the role involve regulatory strategy?
Yes, regulatory strategy and lifecycle management are part of the responsibilities.

Will the role involve safety reporting?
Yes, capturing and reviewing safety reports is a key responsibility.

Application Tips
• Highlight clinical development project experience
• Mention regulatory and lifecycle management exposure
• Showcase safety reporting and medical writing expertise
• Emphasize audit/inspection readiness involvement
• Clearly specify MD or DM qualification and years of experience