Handle inbound and outbound calls related to healthcare services. Provide excellent customer service by addressing queries, concerns and complaints professionally.
Develop and execute regulatory strategies, providing leadership and guidance on pharmaceutical regulatory requirements across India and South Asia to support product registrations, market access, launches, lifecycle management, and post-market compliance.
This individual contributor role has task-level responsibility for clinical trial related document collection, compilation, review and approval across all phases of global clinical trials.
Medical Information is a critically important customer-facing function that supports the safe and effective use of pharmaceutical company products by providing timely, scientifically balanced, evidence based, nonpromotional information in response to unsolicited requests from healthcare professionals, patients, caregivers, and payers
First class post-graduate degree (including integrated PG degree) such as M.S. (Pharm) / M.Pharm or Equivalent (with specialization in Pharmacology & Toxicology/Regulatory Toxicology/Biotechnology. NIPER
Masters / Postgraduate degree in Pharmaceutical Chemistry, Chemistry, or a related discipline, with 03 years of post-qualification experience. National Drug Dependence Treatment Centre (NDDTC), AIIMS, New Delhi