CRA / Sr CRA

<h2>Job Overview:</h2><p style="margin: 0in; margin-bottom: .0001pt;"><span style="font-family: 'Verdana',sans-serif; color: black;">Are you ready to redefine what’s possible, and discover your extraordinary potential at Covance? A career here provides the unique chance to create a lasting impact and difference in our patient’s lives. Joining our team will offer you a rewarding career, an opportunity to work in a high-energy & collaborative workplace, along with access to comprehensive benefits. Your work will be meaningful, the patient outcomes are real, and the results are lasting. With the support of exceptional people from across the globe and an energized purpose, you’ll be empowered to own your career journey with mentoring, training and personalized development planning.</span></p><p style="margin: 0in; margin-bottom: .0001pt;"><span style="font-family: 'Verdana',sans-serif; color: black;">Our mission is to help our clients bring the miracles of medicine to market sooner -- join us for your next career move.</span></p><h2>Education/Qualifications:</h2><p style="margin: 0px;">• University or college degree, or certification in a related allied health profession from an<br />appropriately accredited institution (e.g., nursing licensure). An equivalent amount of<br />experience can be substituted as appropriate.<br />• Thorough knowledge of ICH Guidelines and understanding of local regulatory<br />requirements<br />• Thorough knowledge of monitoring procedures<br />• Basic understanding of the clinical trial process<br /><br /></p><h2>Experience:</h2><p style="margin: 0px;">• A minimum of 1 (One) year of Clinical Monitoring experience is preferred, or an<br />equivalent combination of education and experience to successfully perform the key<br />responsibilities of the job can be substituted.<br />• Ability to monitor study sites independently according to protocol monitoring<br />guidelines, SOP, and local regulatory Guidelines<br />• Have a full understanding of the Serious Adverse Event (SAE) reporting, process<br />production of reports, narratives and follow up of SAEs<br />• Good planning, organization and problem-solving abilities<br />• Ability to work with minimal supervision<br />• Good communication and interpersonal skills<br />• Good analytical and negotiation skills<br />• Computer competency<br />• Fluent in local office language and in English, both written and verbal<br />• Works efficiently and effectively in a matrix environment</p>