Bengaluru

Regulatory-Driven Stability Studies: Design, execute, and monitor stability studies in alignment with global regulatory requirements.

Preferred knowledge of other related disciplines e.g. clinical, regulatory affairs, clinical statistics relevant to aggregate report writing and clinical development 

MSc. in Botany / Biotechnology from a recognised University or equivalent with 2 years relevant experience in Research and Development in Industrial / Academic / Research Institutions. CSIR-CIMAP Research Centre

BA / BS degree with at least 3 years clinical trial experience or direct equivalent experience or advanced degree (MS / PhD /PharmD ) with at least 2 years clinical trial experience.

NIMHANS is conducting a Walk in Selection for Postdoctoral Fellow, Junior Research Fellow. Experience in mass spectrometry for metabolomics/proteomics and associated down steam analyses. Enzyme kinetics, immunoblotting, immunocytochemistry

Pharmacovigilance Scientist, Senior Scientist ensures regulatory compliance and safety of Takeda's products by managing large projects, developing innovative solutions, and leading teams. This role contributes to the development and execution of pharmacovigilance strategies, ensuring patient safety and regulatory adherence

Advanced knowledge of Data Management processes and systems. Solid understanding of clinical drug development process and production of Data Management deliverables

Collaborate with lab staff to gather study requirements, test article information, and study design details necessary for study initiation, laboratory assignment, and resource planning.

Bachelors or Masters degree in Pharmaceutical Sciences, Life Sciences, Chemistry, Engineering, Sciences, or a related discipline