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Global Feasibility Lead II (Remote USA)

Laboratory Corporation of America Holdings (Covance)

Raleigh, North Carolina, United States

<h2>Job Overview:</h2><p style="margin: 0px;"><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;"> Accountable for supporting the development, analyses, interpretation and presentation of primary and secondary data in support of operational strategy and planning</span><br /><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;"> Conducts data mining of internal and external databases and initiates/oversees the collection of primary data for use in development of robust strategies for global clinical trials (country/site mix, site selection, enrollment modeling.).</span><br /><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;"> 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 learning to propose effective solutions as appropriate</span><br /><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;"> Actively participates on cross-functional teams that plan, analyze, and present proposals and bid defenses as part of winning new business and maintaining client base.</span><br /><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;"> 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><br /><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;"> Leads cross functional teams in standalone feasibility efforts; responsible for final report creation and delivery, including discussion of findings and recommendations with external clients</span><br /><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;"> 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><br /><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;"> Develops networking abilities and has an ability/willingness to work with individuals across the globe.</span><br /><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;"> Leads and/or contributes to process improvement or special projects within FSS</span><br /><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;"> Lead and/or contributes to development, implementation, and maintenance of systems within FSS</span><br /><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;"> Contributes to best practice for feasibility conduct</span><br /><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;"> Mentors junior team members (GFL1 or newer GFL2s as needed)</span><br /><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;"> Performs any other duties as assigned</span></p><h2>Education/Qualifications:</h2><p style="margin: 0px;"><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;">Minimum Required:</span><br /><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;"> Qualified candidate has a Bachelor's Degree with equivalent work experience or equivalent years relevant work experience.</span><br /><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;"> 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.<br /></span><br /><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;">Preferred:</span><br /><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;"> Masters degree in science-related discipline preferred</span></p><h2>Experience:</h2><p style="margin: 0px;"><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;"> 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.<br /></span><br /><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;">Preferred:</span><br /><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;"> Understanding of therapeutic drug or device development and marketing</span><br /><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;"> Experience working in an academic, science/health-related industry, or consulting field with responsibilities for the mining, obtaining (across disparate sources), manipulating and presenting of complex scientific data as it relates to clinical research</span><br /><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;"> Relevant industry experience within pharma/biotech, a CRO or consulting firm (or equivalent) is desired</span></p><p style="margin: 0px;"> </p><p style="margin: 0px;"><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;">Position-specific Requirements:</span><br /><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;"> Strong data mining and analytical skills</span><br /><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;"> Strong writing and presentation skills</span><br /><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;"> Upholds the highest standard of personal professionalism and work integrity</span><br /><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;"> Demonstrated ability to work independently</span><br /><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;"> Strong attention to detail/quality control skills</span><br /><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;"> 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><br /><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;"> Ability to establish and maintain effective working relationships with team members, management, operations staff, clients, and executive management</span><br /><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;"> Demonstrated ability to handle multiple competing priorities effectively</span><br /><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;"> Negotiation and relationship management skills</span><br /><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;"> Experience in analysing study and investigator performance metrics</span><br /><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;"> Self-motivated, works effectively under pressure</span></p><p style="margin: 0px;"> </p><p style="margin: 0px;"><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;">Technical Requirements:</span><br /><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;"> Excellent computer skills, including strong working knowledge of Microsoft Office and other data capture and compilation tools</span><br /><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;"> Established knowledge of tools used in obtaining critical market analyses of therapeutic pipelines</span><br /><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;"> Strong skills in scientific data manipulation, analysis, reporting and maintenance</span><br /><span style="font-family: arial,helvetica,sans-serif; font-size: 12pt;"> Proven written and verbal communication skills, with strengths in independently gathering/presenting data in support of operational strategy and planning</span></p>

Job posted: 2021-03-09

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