Karnataka

You will be provided detailed to moderate level of instruction on daily work tasks and detailed instruction on new assignments

Assist senior staff in developing sections of a wide range of pharmacovigilance documents including but not limited to various Periodic Safety Reports, Signal Assessment Reports, Safety Strategy and Core Benefit-Risk Documents, Risk-Management Plans, Patient Safety Narratives and Health Hazard Reports.

Experience in clinical research, pharmacovigilance, or medical monitoring, preferably within a CRO, pharma, or related environment.

Ph.D./ MD/ MS/ MDS or equivalent postgraduate degree. Masters degree in Life Sciences, Health Sciences/ Public Health, Statistics, M. Pharm, M.E., M.Tech or M.Sc. Manipal Academy of Higher Education (MAHE), Manipal

Assist in on-field pilot deployments of innovations through groundwork, requiring travel, stakeholder coordination, liaison with startups, feedback collection, and reporting, etc.

MSc (Life sciences) or M.Sc (Biotech) (3+2 years stream) or MSc Bioinformatics Optional Qualification. Experience in programming (R, Python, or related languages). Institute for Stem Cell Science & Regenerative Medicine, Bangalore

Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company’s integrity & quality standards

Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company’s integrity & quality standards

Solid organizational skills with the ability to adapt and adjust to changing priorities and to manage multiple assignments with challenging/conflicting deadlines