Supports to the Laboratory functions to handle Investigations, Deviation Management, Specifications ,test methods, method validations equipment qualifications ,internal audits and escalations if any.
Post-graduate in Life Sciences (preferably Pharmacy) with minimum of 3 years pharmaceutical industry experience in regulatory affairs with proven track record and experience in health authority interactions and negotiations, end-to-end regulatory submissions
Responsible for triage of Lilly affiliate inquiries and requests and when necessary, consults with CMC RA Scientist for guidance in effort to prepare responses to questions.
Indian citizens and People of Indian origin with PIO status having Ph.D. degree in science, mathematics, engineering, pharmacy, medicine and agriculture related subjects from any recognized university in the world.
Masters Degree / PG Diploma in Life Sciences / Biomedical Sciences / Pharmacy / Public Health / Clinical Research with experience in clinical project management and/or clinical trial/ study monitoring.
Masters degree/ diploma, life sciences, pharmacy, public health, healthcare or other related discipline with a minimum of 2 years of relevant clinical trial monitoring or clinical trial/study coordinator, or clinical trial/study associate experience.
Post Graduate Degree including the integrated PG degrees in relevant subjects: Public Health, Health Economics, Epidemiology, Biostatistics, Pharmaceutical sciences, biomedical engineering
Post Graduate degree from a recognized University in Economics with specialization in Health Economics, Pharmacology, Pharmacy, Public Health, Biotechnology, Biostatistics
Looking for a proactive individual, keen to take on the integral role of Medical Information Specialist within our expanding operation in the UK, working with some of the biggest names in the pharmaceutical industry.