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CMS At ZOLL, we're passionate about improving patient outcomes and helping save lives. We provide innovative technologies that make a meaningful difference in people's lives. Our medical devices, software and related services are used worldwide to diagnose and treat patients suffering from serious cardiopulmonary and respiratory conditions. The Cardiac Management Solutions division of ZOLL Medical Corporation develops products to protect and manage cardiac patients, including the LifeVest wearable cardioverter defibrillator (WCD), the ZOLL cardiac monitor, and associated technologies. Heart disease is the leading cause of death for both men and women in the U.S. At ZOLL, your work will help to ensure cardiac patients get the life-saving therapy they need. To date, the LifeVest WCD has been worn by hundreds of thousands of patients and saved thousands of lives. ZOLL has been Pittsburgh's Manufacturer of the Year, one of Western PA's Healthiest Employers, and even one of Pittsburgh's Coolest Offices. But it's our unique opportunity to impact people's lives that makes ZOLL the ideal place to build your career. Job Summary Responsibility to verify that the rights and well-being of human subjects are protected and that the reported trial data are accurate, complete, and verifiable from source documents. Ensure that the conduct of the trial is in compliance with the currently approved protocol/amendment(s), with GCP, and with applicable regulatory requirements. Identify investigational sites, set up, initiate, monitor and close down the clinical trial. Essential Functions Identify/select suitable investigators who will be responsible for the conduct of the trial at the trial site Act as the main line of communication between the sponsor and the investigator Facilitate investigator contract and budget as required Set up the trial sites, ensuring that all research staff have adequate qualifications and that facilities, investigational products and resources remain adequate throughout Train the site staff to trial-specific industry standards Establish relationships and communicate regularly with investigative site staff and investigators Work with trial sites to develop a subject recruitment plan and assist with subject recruitment and retention initiatives Monitor the trial throughout its duration, which involves visiting the trial sites on a regular basis Verify that the investigator follows the approved protocol, clinical objectives and all GCP/ICH procedures Responsible for subject safety and proper site conduct throughout the trial Verify that source data/documents and other trial records are accurate, complete, and maintained Ensure adverse events, concomitant medications, and inter current illnesses are reported in accordance with the protocol Communicate deviations from the protocol, SOPs, GCP, and the applicable regulatory requirements to the investigator Write visit reports Track, manage and report on trial site status Attend and participate in team meetings to provide status updates and facilitate information sharing File and collate trial documentation and reports Ensure all unused trial supplies are accounted for Close down trial sites on completion of the trial Participate in data reviews Archive study documentation and correspondence Assist with audit preparation and final study reports Required/Preferred Education and Experience Bachelor's Degree in Life Science At least 2 years experience in clinical research At least 2 years experience in medical device/pharmaceutical industry, preferred Cardiovascular device or pharmaceutical experience, preferred Knowledge, Skills and Abilities Well-versed in medical terminology and ICH/GCP guidelines Knowledge of legal and regulatory landscape concerning clinical research Professional use of the English language, bo