Experienced Clinical Research Associate - Multisponsor (Sevilla)

<h1><b><b><b><b><b>Join us in our exciting journey!!</b></b></b></b></b></h1><p></p><p></p><p>We currently require a motivated, creative and enthusiastic clinical trials professional to join our rapidly growing Site Management division.</p><p></p><p>As an experienced <b>Clinical Research Associate</b>, you could be looking to broaden your therapeutic, geographic or study exposure. Or perhaps you are looking a future beyond monitoring with our development opportunities. At IQVIA, you’ll have training and development to plan and progress your career in the direction you choose; we do not believe in a ‘career ceiling.’</p><p></p><p>IQVIA is expanding in Spain - we currently have multiple exciting vacancies for <b> </b><b><b>Clinical Research Associates 2 to work Full Services model</b></b> <b><b>to work with our key pharmaceutical clients</b></b>. If you have independent site monitoring experience as CRA and want to discover how a true partnership between the CRO and sponsor works, then this is the right opportunity for you!</p><p></p><p><u>Our clients are pharmaceutical companies who are dedicated and passionate about improving the lives of patients across several therapeutic areas.</u></p><p></p><p></p><p><b><u>The role: Responsibilities</u></b></p><p></p><ul><li>Perform site selection, initiation, monitoring and close-out visits and work with sites to adapt, drive and track subject recruitment plans.</li><li>Administer protocol and related study training to assigned sites and establish regular lines of communication.</li><li>Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations  – escalating quality issues as appropriate.</li><li>Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrolment, case report form (CRF) completion and submission, and data query generation and resolution.</li><li>Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans</li></ul><p></p><p></p><p><u><b>Our ideal candidate: Skills &amp; other requirements</b></u></p><p></p><ul><li>In depth knowledge and skill in applying applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines</li><li>In depth therapeutic and protocol knowledge as provided in company training</li><li>Excellent organizational and problem-solving skills</li><li>Effective time management skills</li><li>Strong written and verbal communication skills including good command of English and Spanish</li><li><b>Bachelor's degree in a health care or other scientific discipline or educational equivalent</b></li><li><b>2-4 years of independent on-site monitoring experience</b></li></ul><p></p><p></p><p><u><b>What we offer</b></u></p><p></p><ul><li>Working with one of the TOP 5 sponsors globally on international projects.</li><li>Focus on quality, not quantity! We invest in keeping our teams stable, so workload is consistent.</li><li>The chance to work on cutting edge medicines right at the forefront of drug development.</li><li>Genuine career development opportunities for those who want to grow as part of the organization.</li><li>Flexible conditions and an attractive remuneration package.</li><li>Office or home-based roles available! </li></ul><p></p><p></p><p><u><b>We invite you to join IQVIA™</b></u></p><p></p><ul><li>Recognized by <b>Great Place to Work</b> as the second best company to work for in Spain (March 2019)</li><li><b>FORTUNE Magazine's World's Most Admired Companies</b> list for the third year in a row (January 2020)</li><li>Recognized by the 2016 Scrip Awards as the <b>Best Full-service Provider Contract Research Organization</b> (CRO)</li><li>Awarded the 2016 Eagle Award from the Society for Clinical Research Sites (SCRS) for the fourth consecutive year.</li><li>A site-nominated award recognizing contract research organizations (CRO) and biopharmaceutical sponsors dedicated to <b>building positive relationships with research sites through leadership, professionalism and integrity</b>.</li><li>IQVIA™ named in The International Association of Outsourcing Professionals (IAOP) 2017 Global Outsourcing 100® List which recognizes the world’s best service providers across a range of industries.</li></ul><p></p><p></p><p>We know that meaningful results require not only the right approach but also the right people. Regardless of your role, <b>we invite you to reimagine healthcare with us</b>. You will have the opportunity to play an important part in helping our clients drive healthcare forward and whatever your career goals, we are here to ensure you get there!</p><p></p><p>IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelera