Senior Manager, Data Enabled Oncology Recruitment Innovation (Remote)

<h2>Job Overview:</h2><p style="margin: 0in 0in 0pt 14.2pt;"><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;">The primary focus of this role is to support implementation of service offerings that enable patient recruitment for oncology research, leveraging internal capabilities, as well as integration of external vendors. The role will support development of a data enabled recruitment model in oncology. In addition, it will work closely with Site Partnerships to develop and maintain effective site relationships within our data enabled oncology network. The position will forge strong relationships with oncology research sites / networks and external vendors under the leadership of the Director, Data Enabled Oncology Recruitment Innovation.<br /><br /></span></p><ul><li style="color: #000000;"><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;">Support data enabled research network development, as well as rapid site activation model, in addition to other innovations that will create a market leading oncology research community and patient recruitment capability</span></li><li style="color: #000000; font-family: 'Times New Roman',serif; font-size: 11pt;"><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;">Support oncology vendor evaluation, onboarding and qualification, in conjunction with other Feasibility, Recruitment and Engagement members</span></li><li style="color: #000000; font-family: 'Times New Roman',serif; font-size: 11pt;"><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;">Support maintenance of vendor relationships, tracking metrics, use cases, etc. </span></li><li style="color: #000000; font-family: 'Times New Roman',serif; font-size: 11pt;"><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;">Liaise with Diagnostic and Drug Development colleagues to identify and engage with potential data enabled network targets</span></li><li style="color: #000000; font-family: 'Times New Roman',serif; font-size: 11pt;"><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;">Work closely with Site Partnerships to ensure data enablement site relationship is maintained and to optimize study placement</span></li><li style="color: #000000; font-family: 'Times New Roman',serif; font-size: 11pt;"><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;">Work closely with Site Selection and Site Partnerships to ensure selection on relevant opportunities; Start-up to ensure pre-qualification / rapid site activation as a data enabled network site, where applicable; and QA to ensure inspection readiness, regulatory compliance and adherence to ICH GCP, etc. </span></li><li style="color: #000000; font-family: 'Times New Roman',serif; font-size: 11pt;"><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;">Support ongoing review of opportunities to improve site engagement and recruitment services across internal and external capabilities</span></li><li style="color: #000000; font-family: 'Times New Roman',serif; font-size: 11pt;"><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;">Engage with counterparts to identify the value proposition from external data, recruitment and other vendors and link to project teams for trial on active studies and proposal inclusion</span></li><li style="color: #000000; font-family: 'Times New Roman',serif; font-size: 11pt;"><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;">Serve as consultant to Project teams on the implementation of oncology site and recruitment strategies </span></li><li style="color: #000000; font-family: 'Times New Roman',serif; font-size: 11pt;"><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;">Work closely with key stakeholders to resolve issues / escalations</span></li></ul><p style="margin: 0in 0in 0pt 14.2pt;"><span style="font-size: 11pt;"> </span></p><h2>Education/Qualifications:</h2><p style="margin: 0in 0in 0pt;"><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;"><strong>Preferred:</strong></span></p><ul><li style="color: #000000;"><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;">Experience in developing Patient Centric approaches supported by innovative techniques to support clients’ needs.</span></li><li style="color: #000000; font-family: 'Times New Roman',serif; font-size: 11pt;"><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;">High level of business acumen</span></li><li style="color: #000000; font-family: 'Times New Roman',serif; font-size: 11pt;"><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;">Detailed knowledge of CRO and/or Pharmaceutical environment </span></li><li style="color: #000000; font-family: 'Times New Roman',serif; font-size: 11pt;"><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;">Thorough knowledge of relevant Clinical Study Delivery procedures, including Standard Operating Procedures.</span></li><li style="color: #000000; font-family: 'Times New Roman',serif; font-size: 11pt;"><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;">An understanding of aspects surrounding business development (time and cost estimates, bid defense, contracts)</span></li><li style="color: #000000; font-family: 'Times New Roman',serif; font-size: 11pt;"><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;">Proven ability to understand and communicate corporate policies</span></li><li style="color: #000000; font-family: 'Times New Roman',serif; font-size: 11pt;"><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;">Some knowledge of time and cost estimate development and pricing strategies</span></li></ul><h2 style="margin: 0in 0in 0pt;"><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;">Recommended:</span></h2><ul><li style="color: #000000;"><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;">BA/BS required, preferably in life sciences/healthcare from an appropriately accredited institution or equivalent education and experience</span></li><li style="color: #000000; font-family: 'Times New Roman',serif; font-size: 11pt;"><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;">Advanced degree preferred </span></li><li style="color: #000000; font-family: 'Times New Roman',serif; font-size: 11pt;"><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;">Broad knowledge and understanding of global drug development and the clinical trial project management process</span></li><li style="color: #000000; font-family: 'Times New Roman',serif; font-size: 11pt;"><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;">Thorough and practical working knowledge of ICH-GCP Guidelines, including relevant international requirements/guidelines for the conduct of global clinical development programs</span></li></ul><h2>Experience:</h2><h2 style="margin: 0in 0in 0pt;"><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;">Minimum Required:</span></h2><ul><li style="color: #000000;"><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;">8+ years relevant clinical research experience to include a minimum of 5 years in an Oncology related role or 5 years project management or Delivery. </span></li><li style="color: #000000; font-family: 'Times New Roman',serif; font-size: 11pt;"><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;">Minimum of 8 years relevant clinical research experience in Investigational site or relevant research institution, pharmaceutical, or biotech organization</span></li><li style="color: #000000; font-family: 'Times New Roman',serif; font-size: 11pt;"><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;">The ideal candidate will possess 8+ years’ experience with increasing levels of responsibility in a clinical research environment exhibiting strong management skills within and across organizational boundaries.</span></li><li style="color: #000000; font-family: 'Times New Roman',serif; font-size: 11pt;"><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;">Proficient knowledge of oncology landscape, experience with sites and managing relationships, experience with oncology data and oncology vendors</span></li></ul>