The Vice President of Clinical Research (VPCR) will be responsible for overall leadership of clinical research. The VPCR will develop and execute strategic clinical research direction and development activities of Pulsed Electromagnetic Field therapy (PEMF) products and programs. Key clinical activities will include protocol development, IRB submission, study execution and support, clinical data base development and clinical study report authoring and editing. The VPCR will provide scientific expertise to investigators, study teams and vendors and insure that clinical trials follow regulatory and medical requirements. The VPCR will be responsible for strategizing and satisfying regulation requirements to obtain regulatory clearances. The VPCR will work with engineers to discuss and agree on testing standards that must be adhered to as products near commercialization and support the quality department in ensuring that the Company’s standard operating procedures meet and follow the necessary regulations. The VPCR will help plan and write regulatory submissions for product development plans. The VPCR will develop and submit the budget necessary for clinical studies and/or business development plans. Along with the CEO, and other members of the Leadership Team, the VPCR will represent Regenesis Biomedical externally with key stakeholders.
ESSENTIAL DUTIES & RESPONSIBILITIES
This is a high growth, fast paced small organization. The ability to be productive and successful in an intense work environment is critical. Willingness and ability to travel domestically and internationally is required, and it is anticipated that this will be 30% of work time.
Regenesis offers competitive pay, bonus plan, health insurance benefits, matching 401k and a generous paid time off plan.
Regenesis Biomedical is an Equal Opportunity Employer