Clinical Research Scientist
Current- Design studies in nonclinical and preclinical phases, as well as clinical phase I, II, and III studies, to investigate the safety, efficacy, and mechanisms of action of potential drug candidates.
- Analyze preclinical research experiments, including animal models and in vitro assays, to investigate the pharmacological properties and biological effects of drug candidates.
- Operate as project manager to oversee day-to-day operations of multiple studies, ensuring successful execution and oversight of study sites and third-party vendors.
- Write, review, and assist in the submission of regulatory documents and correspondences, including pre-IND submissions, IND submissions, and Orphan Drug Designation applications.
- Write, author, and review abstracts, posters, and manuscripts for publication in scientific journals and presentations at conferences, effectively communicating research findings to both scientific and lay audiences.