Ref #: 30827

Employment type: Permanent - Full-Time

Location: Santiago

Posted: 26-Jul-2021


? Responsible for successful implementation and operational aspects of Phase I to IV clinical studies.
? Direct/lead the Team to ensure successful completion of Phase I, II, III and IV clinical trials in a timely, ethical, and a scientifically responsible fashion.
? Evaluate feasibility of, and direct a program of Phase I, II, III and IV clinical research involving products leading to the filing of an NDA. This entails reviewing protocols and supervising the conduct of clinical studies in adherence of Sanofi SOPs, as well as institutional and relevant governmental regulations.
? Ensure training as required, regarding the product, the pathology, the regulatory environment, the protocol and the CRF.
? Maintain a network of experts and potential investigators within his/her therapeutic field. Identification and evaluation of investigators. Medical representative responsibilities: SAE, narrative summaries;
active collaboration with the corresponding clinical operations department; presentation of the trial, presentation of trial results, provide answers to questions of a medical nature; participation in important congresses or events concerning the therapeutic field.