Job Description
WHY JOIN MILESTONE At Milestone, we aspire to advance and implement paradigm shifts for cardiac therapy. We are currently focused on developing anti-arrhythmia treatments for self-administration outside of the emergency department or hospital setting for patients with acute episodes of paroxysmal supraventricular tachycardia (PSVT) and atrial fibrillation (AFib), as well as other episodic cardiovascular conditions. In addition to our science and innovation, we are a team guided and driven by our core values. Patient needs and empowerments are continually upheld as central to our mission. Our teamwork is strengthened in an environment in which we support and challenge each other while enjoying and celebrating our achievements. We maintain an entrepreneurial, proactive, and action-oriented mindset that places high value on grit, courage, and resolve. Decision-making is based on evaluating information and an idea’s merits; data-driven proposals are both supported and sought. We act individually and as a team with humility, candor, empathy, and unwavering integrity. We have been successful in attracting and empowering best-in-class talent, and we seek those with passion to join on our journey to develop treatments and to motivate change. We are excited about possibilities of this team and what we can accomplish together. YOU WILL BE RESPONSIBLE FOR: Supporting end-to-end clinical trial execution, ensuring delivery against timelines, quality standards, and budget; Assisting in start-up activities of clinical research studies including Investigator site selection; Contributing to development of clinical protocols and study documents including informed consent forms, study logs, study manuals, study plans, case report forms and guidelines; Assisting in development of training materials and training of CRAs and other CRO personnel; Attending co-monitoring and/or training visits at clinical sites as required; Attending and co-monitoring studies (PSV, SIV, IMV, COV) as needed
