Global Medical Science Liaison – Clinical Partnerships

Benefits & Culture

• Medical, dental, and vision insurance for you and your family — from day one.
• Competitive base salary plus performance bonuses and employee stock options.
• Annual learning budget, access to pharma conferences, and paid certifications.
• Opportunities to work across our offices in India, Europe, and Asia-Pacific.
• Mental health support, gym reimbursement, and flexible wellness days.
• 20 weeks fully paid parental leave for primary caregivers, 10 weeks for secondary.

Responsibilities: GMP Quality Assurance and Regulatory Affairs for pharmaceutical manufacturing.

Responsibilities:
Develop and optimise tablet, capsule, and suspension formulations from concept through stability and scale‑up.

Responsibilities:

• Prepare and submit dossiers for FDA, EMA, and WHO‑PQ registrations.
• Manage product lifecycle regulatory activities.
• Build relationships with KOLs and HCPs, communicate clinical evidence, and support medical education activities in assigned territory.

Responsibilities:
Manage end‑to‑end pharmaceutical supply chain, cold‑chain compliance, and distribution partner coordination across 50+ markets.

Responsibilities:
Oversee data collection, cleaning, and validation for Phase II–III clinical trials in compliance with ICH E6 GCP guidelines.