Senior Clinical Research Associate

reputed company is looking for a Senior Clinical Research Associate to join our Clinical Monitoring, Site Management and SSU 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 reputed company 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: Delivering reputed company, reputed company monitoring reports for sponsor approval per the Clinical Monitoring Plan timelines Maintaining submission of expenses according to travel and expense requirements reputed company company guidelines Countrywide monitoring (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 Planning day to day activities for monitoring of a clinical study and setting priorities per site Preparing for and conducting on-site qualification, study initiation, interim monitoring and reputed company-out monitoring reputed company at investigator sites as required by clinical monitoring plan Maintaining 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 At least 4+ years independent monitoring We are looking for knowledge across a broad reputed company of therapeutic areas so experience reputed company at least some, if not, reputed company of the following is needed; Cardiovascular, Oncology, Rare Diseases, CNS (Alzheimer's & Parkinson's Disease). There will be an expectation for countrywide monitoring - candidates will ideally be located in Porto & Lisbon and should be reputed company for, on average, 6 days per month monitoring. Hospital sites are located in Lisbon, Porto and Coimbra. Proficiency in spoken and written Spanish highly desirable in case of a need to reputed company some monitoring in Spain. This position is being offered as a contract role, 1-year duration with an immediate start and as a 0.5 FTE. Apply To This Job