This role is responsible for the clinical operations function, specifically the aspects of planning, initiating, ongoing supervision, and completion of clinical research studies. Additional responsibilities include the management of clinical research projects from clinical development through clinical trials, including the development of clinical protocols, monitoring clinical trials, data collection and reporting. This individual will also be responsible for being the liaison with CROs, clinical sites, and the company stakeholders.
* BA/BS in life sciences
* PMP certification preferred, not required
* Minimum of 8 years experience in clinical operations
* Immunological/anti-inflammatory experience is a plus
This is a fast-paced culture best suited for individuals looking to make a long-lasting impact on an organization where you are free to lead.