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Reporting to the Manager of Clinical Research Associates, the person in this role is responsible for the management of day to day aspects of investigational site activities on assigned clinical trials. The CRA should ensure compliance with international guidelines, local regulations and corporate policies and procedures. Successful candidates will be forward thinking, anticipate needs and be able
Posted 1 day ago
Reporting to the Manager of Clinical Research Associates, the person in this role is responsible for the management of day to day aspects of investigational site activities on assigned clinical trials. The CRA should ensure compliance with international guidelines, local regulations and corporate policies and procedures. Successful candidates will be forward thinking, anticipate needs and be able
Posted 1 day ago
Improve patient outcomes through education and medical staff interaction, including clinical demos and ongoing training for new and existing accounts Collect clinically relevant data, document trip results, and communicate activities with other team members and sales counterparts. Acquire and demonstrate a working knowledge of our products/therapies and develop an extensive understanding of all th
Posted 1 day ago
Improve patient outcomes through education and medical staff interaction, including clinical demos and ongoing training for new and existing accounts Collect clinically relevant data, document trip results, and communicate activities with other team members and sales counterparts. Acquire and demonstrate a working knowledge of our products/therapies and develop an extensive understanding of all th
Posted 1 day ago
Plan, coordinate, and arrange study communications and critical meetings on and off site with both internal and external attendees. Responsible for drafting Meeting Agendas and detailed Meeting Minutes for review and approval by Clinical Project Manager/Clinical Program Manager. Set up, update, maintain and close Trial Master Files. Assures currency and accuracy of required clinical trials documen
Posted 1 day ago
Abiomed is a pioneer and global leader in healthcare technology and innovation, with a mission of Recovering Hearts & Saving Lives . With corporate headquarters in Danvers, Massachusetts, offices in Aachen & Berlin, Germany and Tokyo, Japan, Abiomed's 1,700 employees form one of the fastest growing medical device companies in the world. We attract and retain exceptional talent with our collaborati
Posted 1 day ago
Conversion of user needs and design inputs into software specification. Design, development and test algorithms per medical device software development life cycle (IEC 62304) Participate in software risk analysis and mitigation. Collaborate with cross functional team members, including clinicians, data scientists in further refinement and development of advanced algorithms. Prepare and maintain pr
Posted 1 day ago
Help execute the vision and strategy for Impella Connect and cloud based services at Abiomed. Lead team in writing epics and stories for shared understanding and execution Work with the architects and technical members of the team to ensure that product vision and technical execution are in harmony Maintain internal and external stakeholder analysis and inventory Internalize and deeply understand
Posted 1 day ago
Improve patient outcomes through education and medical staff interaction, including clinical demos and ongoing training for new and existing accounts Collect clinically relevant data, document trip results, and communicate activities with other team members and sales counterparts. Acquire and demonstrate a working knowledge of our products/therapies and develop an extensive understanding of all th
Posted 1 day ago
Improve patient outcomes through education and medical staff interaction, including clinical demos and ongoing training for new and existing accounts Collect clinically relevant data, document trip results, and communicate activities with other team members and sales counterparts. Acquire and demonstrate a working knowledge of our products/therapies and develop an extensive understanding of all th
Posted 1 day ago
Improve patient outcomes through education and medical staff interaction, including clinical demos and ongoing training for new and existing accounts Collect clinically relevant data, document trip results, and communicate activities with other team members and sales counterparts. Acquire and demonstrate a working knowledge of our products/therapies and develop an extensive understanding of all th
Posted 1 day ago
Responsible for comprehensive study management for clinical study, for example protocol and database development, site management project planning, Chair core team meetings for assigned studies ensuring goals and deliverables are clearly defined, and issues, decisions, risks and actions are appropriately tracked Responsible for project development & performance tracking and risk management Maintai
Posted 1 day ago
Manage and execute a highly complex study for a Class III device Effectively manage a study that enrolls high risk patients in a fast paced environment Conduct clinical research programs in accordance with approved project plans Project development, execution & performance tracking (risk management, administration and issue resolution) Comprehensive study management for clinical study, including b
Posted 1 day ago
Assist Associate Director, Clinical Operations with mapping out a comprehensive training program for new hires including the preparation of electronic and paper based on boarding materials. Assist with assessing training needs for new and existing employees as well as external vendors (i.e., core labs, CRO/ARO etc.) and identifying training activities/systems to address competency gaps, as identi
Posted 1 day ago
Receives global cross functional assignments in the form of objectives and determines how to meet schedules and goals. Responsible for the development of all Quality Control Plans/related documents and oversees/performs implementation of quality control activities for assigned projects according to committed timelines. Conducts Quality Control activities which include, but are not limited to the f
Posted 1 day ago
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