Manager Jobs

About The Position

Requirements

• Bachelor’s degree in Biomedical Science, Healthcare or a Life Science related field required.
• 7+ years Clinical Research experience with at least 2 years in a supervisory leadership capacity preferred.
• Demonstrated leadership, ability to effectively communicate and drive positive change.
• Equally adept at running traditional in person and innovative virtual clinical studies.
• Proactively manage LECR and readily adapt to and incorporate new technologies and platforms.
• Successfully multi-task in an entrepreneurial environment and manage multiple clinical studies in parallel.

Nice To Haves

• Advanced degree (MSN/NP, MD, DO, PharmD, MHSA, PhD) preferred.

Responsibilities

• 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.
• 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.
• 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.
• 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.
• Primary point of contact for the IRB.
• Prepares and manages all LE Clinical Research budgets.
• Sets priorities for all staff to assure project timelines are met, including active promotion of clinical research initiatives, i.e. use of social media.
• 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.
• Responds to inquiries from individuals seeking funding or product donations, and if warranted, presents project and recommendations to administration.
• 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.
• Supports the study team with the various tasks associated with conducting the clinical trial to ensure goals are met.
• Seeks out ways to employ innovative technology to optimize organization and individual efficiency and performance.
• Proactively drives the effort to achieve the goal of creating an impactful Clinical Center of Excellence.
• Hires, trains and assures high quality supervision of the LE clinical research staff.
• 2 onsite days per week is an essential function of this position with flexibility to work additional onsite days as needed.
• Travels as needed.
• Additional duties as assigned.