Director, Clinical Research

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    "requisitionDescription": "<table border=\"1\" cellspacing=\"0\" cellpadding=\"0\" width=\"666\" style=\"margin-left: -13.75pt;\" data-pasted=\"true\"><tbody><tr><td valign=\"top\" style=\"width: 100%;\"><p style=\"margin-left:0in;\"><u>General Description:</u> Leads Life Extension Clinical Research and ensures studies are conducted in a timely, quality driven manner while following all applicable guidelines. This role is responsible for the day-to-day operations of Life Extension Clinical Research, including managing clinical studies (onsite and virtual) with a sense of urgency, within budget and with the goal of creating a Clinical Center of Excellence.</p></td></tr><tr><td valign=\"top\" style=\"width: 100%;\"><p style=\"margin-left:0in;\"><strong><u>Core Duties and Responsibilities:</u></strong></p><div style=\"margin-left:0in;\"><ul style=\"list-style-type: disc;margin-left: 0in;\"><li style=\"margin-left:0in;\">Provides overall leadership to LECR and staff by clearly communicating goals and expectations and driving productivity with a sense of urgency while ensuring 100% compliance with rules and regulations.</li><li style=\"margin-left:0in;\">Ensure all clinical trial projects (internal and external), to include project management, tracking and reporting trial progress and monitoring test item expiration dates in relation to project timelines&nbsp;</li><li style=\"margin-left:0in;\">Management and oversight of research projects and laboratory components of studies; develops appropriate study design and establishes accurate timelines; collaborates on statistical plans and data analysis</li><li style=\"margin-left:0in;\">Prepares and/or supervises the preparation of the Protocol, Informed Consent and associated documentation for clinical studies and assures necessary project approvals from an Institutional Review Board (IRB) are obtained</li><li style=\"margin-left:0in;\">Primary point of contact for the IRB</li><li style=\"margin-left:0in;\">Prepares and manages all LE Clinical Research budgets</li><li style=\"margin-left:0in;\">Sets priorities for all staff to assure project timelines are met, including active promotion of clinical research initiatives, i.e. use of social media</li><li style=\"margin-left:0in;\">Assures all applicable regulations are implemented and followed; supervises management of data files and confidential information; follows established SOPs, i.e. for appropriate document destruction&nbsp;</li><li style=\"margin-left:0in;\">Responds to inquiries from individuals seeking funding or product donations, and if warranted, presents project and recommendations to administration</li><li style=\"margin-left:0in;\">Monitors progress of ongoing external projects that received Life Extension support and/or donated materials, assuring resupply so materials do not expire without replacement during a project</li></ul></div><ul type=\"disc\"><li style=\"margin-left:0in;\">Supports the study team with the various tasks associated with conducting the clinical trial to ensure goals are met</li><li style=\"margin-left:0in;\">Seeks out ways to employ innovative technology to optimize organization and individual efficiency and performance</li><li style=\"margin-left:0in;\">Proactively drives the effort to achieve the goal of creating an impactful Clinical Center of Excellence.</li></ul><div style=\"margin-left:0in;\"><ul style=\"list-style-type: disc;margin-left: 0in;\"><li style=\"margin-left:0in;\">Hires, trains and assures high quality supervision of the LE clinical research staff</li></ul></div><ul type=\"disc\"><li style=\"margin-left:0in;\">2 onsite days per week is an essential function of this position with flexibility to work additional onsite days as needed</li></ul><div style=\"margin-left:0in;\"><ul style=\"list-style-type: disc;margin-left: 0in;\"><li style=\"margin-left:0in;\">Travels as needed</li><li style=\"margin-left:0in;\">Additional duties as assigned</li></ul></div><p style=\"margin-left:0in;\"><strong><u>Position Requirements:</u></strong></p><div style=\"margin-left:0in;\"><ul style=\"list-style-type: disc;margin-left: 0in;\"><li style=\"margin-left:0in;\">Bachelor&rsquo;s degree in Biomedical Science, Healthcare or a Life Science related field required; Advanced degree (MSN/NP, MD, DO, PharmD, MHSA, PhD) preferred</li><li style=\"margin-left:0in;\">7+ years Clinical Research experience with at least 2 years in a supervisory leadership capacity preferred</li><li style=\"margin-left:0in;\">Demonstrated leadership, ability to effectively communicate and drive positive change&nbsp;</li><li style=\"margin-left:0in;\">Equally adept at running traditional in person and innovative virtual clinical studies.</li><li style=\"margin-left:0in;\">Proactively manage LECR and readily adapt to and incorporate new technologies and platforms</li><li style=\"margin-left:0in;\">Successfully multi-task in an entrepreneurial environment and manage multiple clinical studies in parallel</li></ul></div></td></tr></tbody></table>\n",
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