Sr Global Feasibility Lead

<h2>Job Overview:</h2><ul style="margin-top: 0in;"><li style="color: black;"><span style="font-size: 11.0pt;">Accountable and takes ownership of the development, analyses, interpretation and presentation of primary and secondary data in support of operational strategy and planning </span></li><li style="color: black;"><span style="font-size: 11.0pt;">Conducts data mining of internal and external databases and initiates/oversees the collection of primary data for use in development of robust strategies for high-profile, large, complex clinical trials (country/site mix, site selection, enrollment modeling.).</span></li><li style="color: black;"><span style="font-size: 11.0pt;">Participates in the development of proposals and bid defenses; provides recommendations on the most appropriate use of data to support proposals and bid defense presentations, works with the team to identify potential risks, and is able to propose effective solutions as appropriate</span></li><li style="color: black;"><span style="font-size: 11.0pt;">Able to independently participate on cross-functional teams that plan, analyze, and present proposals and bid defenses as part of winning new business and maintaining client base. </span></li><li style="color: black;"><span style="font-size: 11.0pt;">Serves as functional bidder reviewer of the budget and text for proposals for which feasibility and/or site identification is included as the primary deliverable</span></li><li style="color: black;"><span style="font-size: 11.0pt;">Able to independently lead cross functional teams in standalone feasibility efforts; responsible for final report creation and delivery, including discussion of findings and recommendations with external clients</span></li><li style="color: black;"><span style="font-size: 11.0pt;">Participates in intra and inter-departmental meetings, leading/contributing to the presentation of information on feasibility offerings, demonstrating continued value-add of the department and providing training on best practices, processes and tools.</span></li><li style="color: black;"><span style="font-size: 11.0pt;">Develops networking abilities and has an ability/willingness to work with individuals across the globe. </span></li><li style="color: black;"><span style="font-size: 11.0pt;">Develops and leads process improvement or special projects within FSS</span></li><li style="color: black;"><span style="font-size: 11.0pt;">Leads development, implementation, and maintenance of systems within FSS</span></li><li style="color: black;"><span style="font-size: 11.0pt;">Expected to serve as a SME for specific FSS tools, systems, and processes, or within a therapeutic area</span></li><li style="color: black;"><span style="font-size: 11.0pt;">Develop and implements best practice for feasibility conduct</span></li><li style="color: black;"><span style="font-size: 11.0pt;">Mentors junior team members (GFL1 & GFL2)</span></li><li style="color: black;"><span style="font-size: 11.0pt;">Performs any other duties as assigned</span></li></ul><h2>Education/Qualifications:</h2><h2>Minimum Required:</h2><ul><li style="margin-left: .25in;"><span style="font-size: 11.0pt;">Qualified candidate has at least a bachelor's degree with  work experience or equivalent years relevant work experience at minimum</span></li><li style="margin-left: .25in;"><span style="font-size: 11.0pt; color: black;">Practical experience and understanding of global drug development and clinical trials including demonstrated experience for the mining, manipulating and presenting of complex scientific data as it relates to clinical research and market analyses. </span></li></ul><p style="margin-left: .25in;"><span style="font-size: 11.0pt; color: black;"> </span></p><h2>Preferred:</h2><ul><li style="margin: 0in 8.8pt .0001pt .25in;"><span style="font-size: 11.0pt;">Master degree in science-related discipline </span></li><li style="margin-left: .25in;"><span style="font-size: 11.0pt; color: black;">Understanding of therapeutic drug or device development and marketing.</span></li><li style="margin: 0in 8.8pt .0001pt .25in;"><span style="font-size: 11.0pt;">Minimum of 5 years in an academic, science/health-related industry (including CRO, investigator site or pharma/biotech), or consulting field with responsibilities for the mining, manipulation and presenting of complex scientific data as it relates to clinical research or equivalent</span></li></ul><h2>Experience:</h2><p style="margin: 0px;"><strong><span style="font-size: 11.0pt;">Minimum</span></strong></p><ul><li style="margin: 0in 8.8pt .0001pt .25in;"><span style="font-size: 11.0pt;">Practical experience and understanding of global drug development and clinical trials including demonstrated experience for the mining, manipulating and presenting of complex scientific data as it relates to clinical research and market analyses. </span></li></ul><p style="margin: 0px;"><strong><span style="font-size: 11.0pt;">Preferred:</span></strong></p><ul><li style="margin: 0in 8.8pt .0001pt .25in;"><span style="font-size: 11.0pt;">Understanding of therapeutic drug or device development and marketing </span></li><li style="margin: 0in 8.8pt .0001pt .25in;"><span style="font-size: 11.0pt;">Minimum of 5 years in an academic, science/health-related industry (including CRO, investigator site or pharma/biotech), or consulting field with responsibilities for the mining, manipulation and presenting of complex scientific data as it relates to clinical research or equivalent</span></li></ul><p style="margin: 0in 8.8pt .0001pt .25in;"><span style="font-size: 11.0pt;"> </span></p><p style="margin-left: .5in;"> </p><p style="margin-right: 8.8pt;"><strong><span style="font-size: 11.0pt;">Position-specific Requirements:</span></strong></p><ul><li style="margin: 0in 8.8pt .0001pt .25in;"><span style="font-size: 11.0pt;">Strong data mining and analytical skills</span></li><li style="margin: 0in 8.8pt .0001pt .25in;"><span style="font-size: 11.0pt;">Strong writing and presentation skills</span></li><li style="margin: 0in 8.8pt .0001pt .25in;"><span style="font-size: 11.0pt;">Upholds the highest standard of personal professionalism and work integrity </span></li><li style="margin: 0in 8.8pt .0001pt .25in;"><span style="font-size: 11.0pt;">Demonstrated ability to work independently</span></li><li style="margin: 0in 8.8pt .0001pt .25in;"><span style="font-size: 11.0pt;">Strong attention to detail/quality control skills </span></li><li style="margin: 0in 8.8pt .0001pt .25in;"><span style="font-size: 11.0pt;">Ability to participate in a lead role in client facing meetings, e.g. bid defences or capabilities meetings</span></li><li style="margin: 0in 8.8pt .0001pt .25in;"><span style="font-size: 11.0pt;">Ability to successfully and quickly understand scientific information so as to be able to independently source data/information relevant to a scientific/medical strategy </span></li><li style="margin: 0in 8.8pt .0001pt .25in;"><span style="font-size: 11.0pt;">Ability to establish and maintain effective working relationships with team members, management, operations staff, clients, and executive management </span></li><li style="margin: 0in 8.8pt .0001pt .25in;"><span style="font-size: 11.0pt;">Ability to inspire, to lead by example and motivate and negotiate with teams to seek solutions and get results </span></li><li style="margin: 0in 8.8pt .0001pt .25in;"><span style="font-size: 11.0pt;">Demonstrated ability to handle multiple competing priorities effectively</span></li><li style="margin: 0in 8.8pt .0001pt .25in;"><span style="font-size: 11.0pt;">Strong understanding and experience in operationalizing clinical development programs in a global setting</span></li><li style="margin: 0in 8.8pt .0001pt .25in;"><span style="font-size: 11.0pt;">Strong negotiation and relationship management skills</span></li><li style="margin: 0in 8.8pt .0001pt .25in;"><span style="font-size: 11.0pt;">Experience in analysing study and investigator performance metrics </span></li><li style="margin: 0in 8.8pt .0001pt .25in;"><span style="font-size: 11.0pt;">Ability to translate complex business questions and requirements and develop effective solutions</span></li><li style="margin: 0in 8.8pt .0001pt .25in;"><span style="font-size: 11.0pt;">Strong business acumen</span></li><li style="margin: 0in 8.8pt .0001pt .25in;"><span style="font-size: 11.0pt;">Self-motivated, works effectively under pressure</span></li></ul><p style="margin-right: 8.8pt;"><strong><span style="font-size: 11.0pt;"> </span></strong></p><p style="margin-right: 8.8pt;"><strong><span style="font-size: 11.0pt;">Technical Requirements:</span></strong></p><ul><li style="margin: 0in 8.8pt .0001pt .25in;"><span style="font-size: 11.0pt;">Excellent computer skills, including strong working knowledge of Microsoft Office and other data capture and compilation tools </span></li><li style="margin: 0in 8.8pt .0001pt .25in;"><span style="font-size: 11.0pt;">Established knowledge of tools used in obtaining critical market analyses of therapeutic pipelines</span></li><li style="margin: 0in 8.8pt .0001pt .25in;"><span style="font-size: 11.0pt;">Strong skills in scientific data manipulation, analysis, reporting and maintenance </span></li><li style="margin: 0in 8.8pt .0001pt .25in;"><span style="font-size: 11.0pt;">Proven written and verbal communication skills, with strengths in independently gathering/presenting data in support of operational strategy and planning </span></li></ul>