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EDS Reviewer

Laboratory Corporation of America Holdings (Covance)

San José, Costa Rica

<h2>Job Overview:</h2><p style="margin: 0px;"><span style="font-size: 12pt;"><span style="font-family: Arial, sans-serif;">Get ready to redefine what’s possible and discover your extraordinary potential at Covance. Here, you’ll have the opportunity to personally advance healthcare and make a difference in peoples’ lives with your bold ideas and unique point of view. 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><span style="font-family: 'Times New Roman', serif;"><br /><br /></span><span style="font-family: Arial, sans-serif;">Join us as we speed the delivery of groundbreaking therapies and anticipate tomorrow’s drug development challenges, creating new possibilities for our clients—and your career.</span></span></p><p style="margin: 0px;"><span style="font-size: 12pt;"><strong><span style="font-family: Arial, sans-serif;">COVANCE</span></strong><span style="font-family: Arial, sans-serif;"> is a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries. We have an exciting opportunity available to join our team.</span></span></p><p style="margin: 0px;"><span style="font-size: 12pt;"><span style="font-family: 'Times New Roman', serif;"><br /></span><span style="font-family: Arial, sans-serif;">We are currently recruiting an <strong>External Data Specialist in Costa Rica</strong></span></span></p><h2>Education/Qualifications:</h2><ul><li><span style="font-size: 11.0pt;">Associates or bachelor’s degree in Medical/Life Science/Computer Science or equivalent combination of education and experience to successfully perform the key responsibilities of the job.</span></li></ul><h2>Experience:</h2><h2>Minimum Required:</h2><ul><li style="margin-left: .5in;"><span style="font-size: 11.0pt;">4 years prior experience in the pharmaceutical, biotechnology, medical device/diagnostics, or clinical trial industries or an equivalent combination of education and experience to successfully perform the key responsibilities of the job.</span></li><li style="margin-left: .5in;"><span style="font-size: 11.0pt;">Project Management experience strongly preferred. Basic understanding of medical terminology a plus.</span></li><li style="margin-left: .5in;"><span style="font-size: 11.0pt;">Strong organizational, planning, and critical-thinking skills.</span></li><li style="margin-left: .5in;"><span style="font-size: 11.0pt;">Well-polished, inclusive, and engaging communication skills (written and verbal) to support effective interactions with sponsors and internal colleagues.</span></li><li style="margin-left: .5in;"><span style="font-size: 11.0pt;">Strong negotiation skills to facilitate, guide, influence, and produce a unified approach within a global, cross-functional environment.</span></li><li style="margin-left: .5in;"><span style="font-size: 11.0pt;">Ability to handle multiple tasks in a timely and professional manner under demanding conditions.</span></li><li style="margin-left: .5in;"><span style="font-size: 11.0pt;">Ability to use standard Microsoft suite of software products.</span></li><li style="margin-left: .5in;"><span style="font-size: 11.0pt;">Strong technical aptitude.</span></li><li style="margin-left: .5in;"><span style="font-size: 11.0pt;">Ability to maintain confidentiality of data and information during interaction with staff at all levels.</span></li><li style="margin-left: .5in;"><span style="font-size: 11.0pt;">Understanding of ICH-GCP principles.</span></li></ul>

Job posted: 2021-07-06

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