Be part of a team that is transforming care for people with heart and vascular disease
Innovation is at the core of our ethos. It drives our mission to deliver transformative care. We are committed to the highest quality in all that we do through collaboration among our highly skilled, experienced professionals.
Every team member is greatly valued and shares the vision of significantly improving treatment paradigms. We lean on each other, support one another and hold ourselves accountable to each other. Every member of our team is a key contributor to our success.
Taking care of our team
We appreciate and recognize the brilliance of our team members.
Competitive benefits and perks are just two of the ways that we show our appreciation.
Comprehensive health care options
401(k) with available Roth contributions
Commuter & transit program
Paid time off + 11 company holidays annually
Free coffee, tea, fruit and snacks
Join us in transforming care for people with heart and vascular disease.
The Manager/Director, Clinical Research is responsible for leading and driving clinical trial execution for multiple studies to ensure all assigned trial deliverables across programs are completed according to timelines, budget, applicable regulations, quality standards, SOPs and business guidelines. This individual will be a strategic thinker, problem-solver and is accountable for identifying risks and developing risk mitigation strategies. Must demonstrate significant expertise in the successful planning, implementation, and execution of a broad portfolio of global clinical trial operations. Exceptional critical thinking and problem-solving is a must.
Manager, Clinical Data Management Major Duties and Responsibilities
Responsibilities will include, but not be limited • Serve as the domain expert in providing clinical data management and electronic data capture (EDC) expertise to support clinical studies
• Design the case report forms (CRFs) in collaboration with the clinical operations team according to clinical protocol and study data requirements
Clinical Research Associate Major Duties and Responsibilities
Responsibilities will include, but not be limited to ensures timely collection of study documentation by obtaining, maintaining, and controlling all necessary records and documentation according to procedures and regulations Maintains documentation in the Trial Master File (TMF) for all assigned clinical studies according to internal procedures and regulations. Duties may include electronic and hardcopy file maintenance [….]