August 2025

Responsible for leading and managing applications through the regulatory approval process, including preparation of Post Approval Submissions to Health Canada, to obtain timely approvals

Clinical Scientist will be responsible for design and execution of assigned clinical trial activities and work closely with clinical team members within the assigned project to execute activities associated with the conduct

The incumbent will be responsible for performing analytical method development and validations for USP/NF monographs and maintaining safety and GLP environment in the lab.

To have an oversight on CRO partners for outsourced studies by conducting oversight quality visits at sites if applicable, conduct regular meetings and seek regular updates on study progress.

Providing balanced, objective, and accurate information to regulators, the scientific community, health care professionals, payers, and patients in a consistent and timely fashion across the entire drug development lifecycle is fundamental to Lilly.

Lead scientific engagement with their Medical Experts. Implement clinical and educational strategies and respond to unsolicited medical enquiries.

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.

M.Sc. in Chemical sciences, Life sciences OR Master of Pharmaceutical Sciences in Pharmaceutical chemistry, Natural Products OR M.Tech in Biotechnology, Nanoscience and Nanotechnology.

Masters in Natural or Agricultural or Pharmaceutical Sciences/MVSc/Animal Sciences OR Bachelors degree in Engineering or Technology or Medicine from a recognized University