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Start-Up Specialist/ Sr Start-Up Specialist

Laboratory Corporation of America Holdings (Covance)

Buenos Aires, Argentina

<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 LabCorp? 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;">Recommended:<br />Level of education preferred (if required or experience level which may be substituted for level of education).<br />Professional degree/designations/certifications/licenses legally required (i.e. RN, MD, VDM etc.).<br /> University/College degree (life science preferred), or certification in a related allied health profession from an appropriate accredited institution (e.g., nursing certification, medical or laboratory technology) AND 2 years work experience in clinical research, including a strong working knowledge of the ICH guidelines and FDA, IRB/IEC regulations.<br /> In lieu of the above requirement, candidates with a High School Diploma or equivalent AND a minimum of 2 years work experience in clinical research, including a strong working knowledge of the ICH guidelines and FDA, IRB/IEC regulations will be considered.</p><h2>Experience:</h2><p style="margin: 0px;">Minimum Required:<br /> Minimum of 2 years of experience in clinical development or start up/ regulatory process.<br /> Working knowledge of ICH, FDA, IRB/IEC and other applicable regulations/guidelines; familiarity with investigator start-up documents and contract/budgets negotiation process; previous interaction with operational project teams and investigative sites<br /> Demonstrated understanding of research protocol requirements and proven ability to communicate them/educate others about them</p>

Job posted: 2021-10-12

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