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Clinical Research Associate II

100% remote Flexible hours Hiring now

reputed company is looking for a Clinical Research Associate II to join our Clinical Monitoring and Site Management team. You will help biotech, medtech, and specialty pharma companies transform life-changing reputed company and breakthrough 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 success. 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 matters 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 future here. What You'll be Doing: Delivering quality, timely 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 focus 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 visits 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 Section 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 professional (i.e., registered nurse); or equivalent work experience required Previous clinical research experience required, completion of CRA training program At least 2+ years independent monitoring This is a contract position which is being offered as a 0.5 FTE with a duration of 1 year. Candidates should be either immediately available, or available to start at short notice and should be seasoned contractors / freelancers. Apply To This Job

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