Perform method development, method validation and study sample analysis in compliance with applicable method, protocol, SOPs and regulatory guidelines.
Maintain robust governance for label changes triggered by safety signals, clinical/CMC updates, and regulatory intelligence; ensure harmonized global implementation timelines and traceability.
MedPlus One of the most trusted gateways to medicines and general provision With an aim to eradicate fake and ineffective medicines, and supply high-quality medicines in India, MedPlus was launched in 2006 in Hyderabad.
Bachelors in life science/healthcare required; Advanced degree or equivalent education / degree in life sciences / healthcare preferred (PhD/MD/PharmD/ Masters).
Looking for a Clinical Data Management Professional who thrives in a dynamic, international environment and brings a strong commitment to data quality and regulatory compliance.