As aStudy Clinical Lead,you’llplay a pivotal role in channeling our scientific capabilities to make a positive impact on changing patients’ successfulStudy Clinical LeadinLate PhaseCVRM (Cardiovascular, Renal, and Metabolic diseases)will be responsible for the design, conduct, monitoring, data interpretation and reporting of individual clinical trials ensuring that the clinical data collected within the study will allow determination of the benefits and risks of the compound, as well as will allow for the intended label indication and price in markets individual willoperateaccording to the highest ethical standards in compliance with internal SOPs, local regulations, laws,Good Clinical Practice,and regulatory requirements.

Responsibilities