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Manager, Clinical Team Leads

Laboratory Corporation of America Holdings (Covance)

Brazil

<h2>Job Overview:</h2><p style="margin: 0px;"><span style="font-size: 12pt;"><strong>Are you ready to discover you next career Labcorp?</strong></span></p><p style="margin: 0px;"> </p><p style="margin: 0px;"><span style="font-size: 12pt;"><strong>A career at Labcorp provides our employees the unique chance to create an immediate impact and difference in our patient’s lives.</strong></span></p><p style="margin: 0px;"> </p><p style="margin: 0px;"><span style="font-size: 12pt;">will offer a rewarding career, a chance to work in an energetic & team oriented work place, and access to competitive benefits. With the support of exceptional people from across the globe and a vast array of career options, you’ll be empowered to own your career journey with mentoring, training and personalized development planning. </span></p><p style="margin: 0px;"><span style="font-size: 12pt;">                                        </span></p><p style="margin: 0px;"><span style="font-size: 12pt;">Covance by Labcorp is a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries.</span></p><p style="margin: 0px;"> </p><p style="border: none; padding: 0in;"><span style="font-size: 12pt;">We are recruiting for our Team in Latin America are currently seeking to hire a CTL Manager</span></p><p style="border: none; padding: 0in;"> </p><p style="margin-bottom: .0001pt;"><span style="font-size: 12pt;"><span style="font-family: Verdana, sans-serif;">The</span> <span style="font-family: Verdana, sans-serif;">SCPDM will be responsible for both line management and portfolio delivery. The SCPDM will work with the CTLs assigned to a TA/Client portfolio to provide consistent oversight and delivery across the TA/Client studies.</span></span></p><p style="margin: 0px;"><span style="font-size: 12pt; font-family: Verdana, sans-serif;"> </span></p><h2>Education/Qualifications:</h2><p style="margin-bottom: .0001pt;"><span style="font-size: 12pt;"><strong><span style="font-family: Verdana, sans-serif;">Required:</span></strong></span></p><ul><li style="margin-bottom: .0001pt;"><span style="font-size: 12pt; font-family: Verdana, sans-serif;"> University/college degree (life science preferred) or certification in a related allied health profession (i.e. nursing, medical or laboratory technology) from an appropriately accredited institution.</span></li></ul><p style="margin-bottom: .0001pt;"><span style="font-size: 12pt; font-family: Verdana, sans-serif;"> </span></p><p style="margin-bottom: .0001pt;"><span style="font-size: 12pt;"><strong><span style="font-family: Verdana, sans-serif;">Preferred:</span></strong></span></p><ul><li style="margin-bottom: .0001pt;"><span style="font-size: 12pt; font-family: Verdana, sans-serif;"> Masters or other advanced degree.</span></li><li><span style="font-size: 12pt; font-family: Verdana, sans-serif;"> PMP certification</span></li></ul><h2>Experience:</h2><p style="margin-bottom: .0001pt;"><span style="font-size: 12pt;"><strong><span style="font-family: Verdana, sans-serif;">Minimum Required:</span></strong></span></p><ul><li style="margin-bottom: .0001pt;"><span style="font-size: 12pt; font-family: Verdana, sans-serif;">Minimum of six (6) years relevant clinical research experience in a pharmaceutical</span></li></ul><p style="margin-bottom: .0001pt;"><span style="font-size: 12pt; font-family: Verdana, sans-serif;">company/CRO, including at least two (2) years of CTL or equivalent combination of</span></p><p style="margin-bottom: .0001pt;"><span style="font-size: 12pt; font-family: Verdana, sans-serif;">experience to successfully perform the responsibilities of the job.</span></p><ul><li style="margin-bottom: .0001pt;"><span style="font-size: 12pt; font-family: Verdana, sans-serif;">In lieu of the above requirement, candidates with (a) six (6) years supervisory experience in aheath care setting and (b) five (5) years clinical research experience including one (1) years of project management experience (international clinical trial management experience preferred) in the pharmaceutical or CRO industries will be considered</span></li></ul><p style="margin-bottom: .0001pt;"><span style="font-size: 12pt; font-family: Verdana, sans-serif;"> </span></p><ul><li><span style="font-size: 12pt;"><strong><span style="font-family: Verdana, sans-serif;">Preferred:</span></strong></span></li></ul><p style="margin: 0px;"><span style="font-size: 12pt; font-family: Verdana, sans-serif;">Global clinical project management experience.</span></p>

Job posted: 2021-08-31

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