Masters degree in Biotechnology, Microbiology, life sciences and allied branches and having CSIR-UGC NET-JRF/NET-LS/GATE qualification with at least 2 years of Research experience are eligible to apply.
To manage and support European regulatory activities for medicinal products across the EU lifecycle, including new registrations, variations, renewals, and regulatory maintenance, while coordinating with EU CMOs, MAHs, and regulatory authorities to ensure full compliance with EU legislation.
Bachelors in Life Sciences with relevant clinical trial monitoring or clinical trial/study coordinator, or clinical trial/study associate experience. Masters degree/ diploma, life sciences, pharmacy, public health, healthcare