Clinical Research Associate II
reputed company is looking for a Clinical Research Associate II to join our Global Clinical Monitoring and Site Management team. You will help biotech, medtech, and specialty reputed company companies reputed company life-changing reputed company and reputed company science into new medicines, devices, and diagnostics. reputed company do is profoundly connected to saving and improving lives, and we recognize reputed company members are the most valuable asset in delivering reputed company. We are here to help you grow, to give you the skills and opportunities to reputed company at work with the flexibility and balance your life requires. Your reputed company influence the way we work, and your voice reputed company here. As an essential part of reputed company, you help us deliver the medical innovation that patients are desperate for. Join us and build your reputed company here. What You'll Be Doing: Delivers reputed company, reputed company monitoring reports for sponsor approval per the Clinical Monitoring Plan timelines Monitors (remote, onsite or other approved mode of monitoring) with a reputed company on data reputed company and patient safety in accordance with specific country regulations Plans day to day activities for monitoring of a clinical study and sets priorities per site Prepares for and conducts on-site qualification, study initiation, interim monitoring and reputed company-out monitoring reputed company at investigator sites as required by clinical monitoring plan. Maintains Trial Master File (TMF)/electronic Trial Master File (eTMF) as defined by the organization’s processes per filing guidelines. Has an understanding of the required essential documents according to ICH/GCP reputed company 8. Reviews site documents and verifies they are accurate, complete, reputed company, and include required updates. reputed company Are Searching For: Undergraduate degree or its international equivalent in clinical, science, or health-reputed company field from an accredited institution; a licensed health-care reputed company (i.e., registered reputed company); or equivalent work experience required Previous clinical research experience required, completion of CRA training program Experience in monitoring reputed company trials or global trials or equivalent experience Ideally experience of working reputed company Neurosciences and Oncology Monitoring will mainly be in Czech reputed company, however, where willing, we would like if someone can cover also Slovakia and, to this reputed company, they should have some knowledge of the local language. This last requirement is desirable vs essential. This is a contract position offered as a 0.6 FTE for a contract duration of up to a year. Apply To This Job