Associate Project Coordinator, Clinical Pharmacology Services

<h2≥Job Overview:</h2≥<p style="margin-bottom: .0001pt;"≥<span style="font-family: arial, helvetica, sans-serif; color: black; font-size: 10pt;"≥Your new employer is Covance by Labcorp, the world’s most comprehensive drug development company, dedicated to improving health and improving lives. Our unique perspectives, built from decades of scientific expertise and precision delivery of the largest volume of drug development data in the world, along with our innovative technology solutions, help our clients identify new approaches and anticipate tomorrow’s challenges as they evolve. We offer opportunities to work on diverse, challenging projects with bright, interesting colleagues while building a flexible and rewarding career. </span≥</p≥<p style="margin-bottom: .0001pt;"≥<span style="font-family: arial, helvetica, sans-serif; color: black; font-size: 10pt;"≥ </span≥</p≥<p style="margin-bottom: .0001pt;"≥<span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;"≥<span style="color: black;"≥This is your chance to become part of a team that helps to bring the miracles of medicine to market sooner.</span≥ <span style="color: black;"≥Excellent opportunity for an <strong≥Associate Project Coordinator</strong≥ to join our Phase I Clinical Research business in Leeds, West Yorkshire on a full-time and permanent basis<strong≥.</strong≥ This is a great opportunity to develop your career within Clinical research/trials and allow you to continue to practice your clinical skills and knowledge. </span≥You will be supporting Project Manager focused on early phase studies. </span≥</p≥<p style="margin-bottom: .0001pt;"≥<span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;"≥ </span≥</p≥<p style="margin-bottom: .0001pt;"≥<span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;"≥<strong≥<u≥Key Responsibilities</u≥</strong≥</span≥</p≥<p style="margin-bottom: .0001pt;"≥ </p≥<p style="margin-bottom: .0001pt;"≥<span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;"≥Your main responsibilities will include but not be restricted to: </span≥</p≥<p style="margin-bottom: .0001pt;"≥ </p≥<ul≥<li≥<span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;"≥Work with a more senior PC or PM in developing study specific documents ( e.g., Project Management Plan, Communication Plan, Investigator Package Plan, Risk Register, Project Specific Training Matrix and any other applicable plans as required), including compliance with client-specific requirements for low complex studies; distributes them to the study team and/or sponsor for review, compiles comments, and routes final documents.</span≥</li≥<li≥<span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;"≥Maintain an internal standardized filing structure for study-related documents; pro-actively maintains documents within the filing structure.</span≥</li≥<li≥<span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;"≥Responsible for project setup activities ( e.g., study ID request, SAS Environment Setup request, eTMF, Study-specific Distribution Lists, etc.).</span≥</li≥<li≥<span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;"≥Attends and assists in the organization of study-related meetings, as required; distributes meeting agendas; maintains and distributes meeting minutes, Project Log, Risk Register, and study team contact lists; participates in client visits as needed.</span≥</li≥<li≥<span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;"≥As directed and with oversight, assists with business improvements initiatives to drive quality, productivity, and continuous improvements across different business units.</span≥</li≥<li≥<span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;"≥Upon PM request and with Associate Project Coordinator (PC) acceptance, may serve as a sponsor and site contact in the absence of the PM, primarily during maintenance phases of routine single and multi-site low-complexity trials.</span≥</li≥<li≥<span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;"≥Assists the PM or a more senior PC with payments per global finance standards.</span≥</li≥<li≥<span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;"≥Assists in the set-up, coordination and maintenance of sponsor/internal training in accordance with applicable SOPs and processes.</span≥</li≥<li≥<span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;"≥Assists in the development of project tools as required for the project ( e.g., screening and enrolment log and development of investigator training).</span≥</li≥<li≥<span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;"≥Assists the PM, or more senior PC as required with feasibility, including providing sites with feasibility questionnaire and tracking responses.</span≥</li≥<li≥<span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;"≥Assists the PM/more senior PC in maintaining overall project trackers, including financial, screening, and vendors.</span≥</li≥</ul≥<p style="margin: 0px;"≥<span style="font-size: 10pt; color: black; font-family: arial, helvetica, sans-serif;"≥Get ready to redefine what’s possible and discover your extraordinary potential at Covance by Labcorp. 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≥</p≥<p style="margin: 0px;"≥ </p≥<p style="margin: 0px;"≥<span style="font-size: 10pt; color: black; font-family: arial, helvetica, sans-serif;"≥<span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;"≥Join us and discover why Covance by Labcorp has been named by Forbes as one of the World's Best Employers 2020 and more than 90% of the top 20 global pharmaceutical companies are repeat customers. We can offer you not only a job, but a stable, long-term international career.</span≥</span≥</p≥<h2≥Education/Qualifications:</h2≥<ul≥<li≥<span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;"≥University/college degree, preferably in a healthcare/scientific field. Specific clinical research experience may be substituted for education.</span≥</li≥</ul≥<h2≥Experience:</h2≥<ul≥<li≥<span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;"≥Knowledge of the clinical trial process with early clinical pharmacology experience preferred.</span≥</li≥<li≥Recent and relevant experience in a research environment.</li≥<li≥Knowledge of protocol designs, study objectives, study procedures, and project-related timelines.</li≥<li≥Knowledge of GCP/ICH Guidelines and applicable Regulatory Authority Guidelines.</li≥</ul≥<p style="margin: 0px;"≥<span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;"≥<span style="font-size: 10pt;"≥<span style="color: black; font-size: 10pt;"≥#LI-SP2</span≥</span≥</span≥</p≥