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Project Manager, Global Clinical Trials - Remote, FSP

Laboratory Corporation of America Holdings (Covance)

Princeton, New Jersey, United States

<h2>Job Overview:</h2><p style="margin-top: 0pt; margin-bottom: 8pt; font-family: Arial; font-size: 10pt; text-align: left;"><span style="font-weight: bold; font-size: 12pt;">Global Clinical Trial Project Manager, Remote - Home-Based </span></p><p style="margin-top: 0pt; margin-bottom: 8pt; font-family: Arial; font-size: 10pt; text-align: left;"><span style="font-weight: bold; font-size: 12pt;">Must have experience in Clinical Trials and in </span><span style="font-weight: bold; font-size: 12pt;">Oncology.</span></p><p style="margin-top: 0pt; margin-bottom: 8pt; font-family: Arial; font-size: 10.0pt;"><span style="font-size: 12pt;">Covance by Labcorp gives you the best <span style="font-weight: bold;">two-for-one </span>opportunity for career growth.   Who doesn’t want twice the perks<span style="color: #1f497d;">? W</span>orking at one of the largest FSP CROs—and partnering with one sponsor with a dedicated therapeutic focus. <span style="font-weight: bold;">You can have it all!</span></span></p><p style="margin-top: 0pt; margin-bottom: 8pt; font-family: Arial; font-size: 10.0pt;"><span style="font-size: 12pt;">Dedicated to an FSP project<span style="color: #1f497d;">,</span> you will bring your specialized discipline to a core team working directly with one sponsor. Whether your specialization is in clinical monitoring, clinical project management, data management, biometrics or pharmacovigilance<span style="color: #1f497d;">,</span> we have an FSP opportunity to match your area of expertise.</span></p><p style="margin-top: 0pt; margin-bottom: 8pt; font-family: Arial; font-size: 10.0pt;"><span style="font-size: 12pt;">You will enjoy the best of both worlds—all the benefits that come along with our Energizing Purpose, Exceptional People and Extraordinary Potential combined with working exclusively with one sponsor and this also comes with the benefit of bringing your strong therapeutic experience to allow your expertise to shine through.</span></p><p style="margin-top: 0pt; margin-bottom: 8pt; font-family: Arial; font-size: 10.0pt;"><span style="font-size: 12pt;">Our FSP model is flexible and scalable. Our teams are collaborative and proactive – a great place for you to continue honing your therapeutic skills and growing and excelling in new and exciting research.</span></p><p style="margin-top: 0pt; margin-bottom: 8pt; font-family: Arial; font-size: 10.0pt;"><span style="font-size: 12pt;">Our reach is global – extending to 60+ countries making us one of the largest FSP CROs. No matter where you are locat<span style="color: #1f497d;">ed</span> on the globe, we have an FSP opportunity for you.</span></p><p style="margin: .5pt 39.9pt .0001pt 0in;"> </p><p style="margin: .5pt 39.9pt .0001pt 0in;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif; color: black;">Typically, under the direction of a Senior Project Manager/Project Director, the Project Manager II oversees and manages domestic, regional and/or projects. Responsibilities typically include managing project teams, communications, risk, scope, schedule, cost, quality, and stakeholders effectively ensuring that variance from plan is proactively and effectively mitigated and client expectations are met The Project Manager is expected to have a working knowledge of drug development and clinical trial execution. The Project Manager also compiles and drives documentation for the project, ensuring the accuracy and quality of regulatory data. </span></p><p style="margin-bottom: .0001pt;"><span style="font-size: 12pt; font-family: Verdana, sans-serif;"> </span></p><table style="width: 725px; margin-left: 5.4pt; border-collapse: collapse; height: 430px;" width="0"><tbody><tr><td style="width: 397.9pt; padding: 0in 5.4pt 0in 5.4pt;" width="699"><p style="margin-bottom: .0001pt;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;"><strong><span style="color: black;">Operational delivery</span></strong></span></p><p style="margin-bottom: .0001pt;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;"> </span></p><ul><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Responsible for project delivery with regards to agreed time, scope, cost and quality</span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif; color: black;">Serve as key client contact for assigned project responsibilities, establishing working relationships with client project teams which result in client satisfaction, operational excellence and thereby increase potential for repeat business</span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">For areas of project responsibility, lead core project team(s) and facilitate team's ability to lead extended project team(s), ensuring effective cross-functional teamwork among project team members including both internal and external stakeholders. Depending on size and scope of project(s), this job duty may be performed in collaboration with a Senior Project Manager and/or Project Director</span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Serve as escalation point for project issues, within area of project responsibility, to internal and external stakeholders, as appropriate</span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Proactively identify and resolve conflicts as needed</span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Understand the project delivery strategy, costing assumptions and resulting budget for assigned project(s)</span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Monitor project scope, schedule and costs to ensure all remain on track with the contract and with financial performance targets. Initiate and implement appropriate actions to proactively manage the change control process both internally and externally</span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif; color: black;">Proactively lead both quality control and risk assurance activities to ensure project deliverables are met according to regulatory, Covance and client requirements</span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Create and manage variance to required project plans. Per SOPs, implement and monitor progress against project plans and revise as necessary. Ensure that all staff allocated to assigned project(s) adheres to professional standards and SOPs, providing performance feedback to team member’s respective supervisors</span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Aid in development and maintenance of key project performance indicators for client specified metrics, ensuring that the KPIs are within scope of the project contract</span></li></ul></td></tr></tbody></table><h2>Education/Qualifications:</h2><ul><li><span style="font-family: arial, helvetica, sans-serif;"><span style="font-size: 16px;">BA/BS or equivalent degree in a relevant discipline.  </span></span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Preferred:</span><ul><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Masters or other advanced degree.</span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">PMP certification.</span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Minimum of 4 years of relevant clinical research experience in a pharmaceutical company/CRO</span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Experience in all phases of study execution</span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Demonstrated leadership of a global clinical trial and management of CROs</span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Experience with electronic quality, compliance and CTMS systems</span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Working knowledge of ICH Guidelines and GCP including international regulatory requirements for the conduct of clinical development programs</span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Broad knowledge of drug development process and client needs</span></li></ul></li></ul><h2>Experience:</h2><p style="margin: 0px;"> </p><ul><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Working knowledge of project management processes</span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Experience managing projects in a virtual environment</span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Demonstrated ability to handle multiple competing priorities and to utilize resources effectively</span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Financial awareness and ability to actively utilize financial tracking systems</span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Demonstrated ability to inspire effective teamwork and motivate staff within a matrix system.</span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Demonstrated ability to lead by example and to encourage team members to seek solutions independently.</span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Excellent communication, planning and organizational skills</span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Ability to work independently</span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Ability to negotiate and liaise with clients in a professional manner</span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Ability to present to staff at all levels</span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Knowledge and understanding of Microsoft office </span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Travel is estimated around 25% </span></li></ul><p style="margin-bottom: .0001pt;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;"> </span></p>

Job posted: 2021-04-26

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