As the flagship higher education institution of The Church of Jesus Christ of Latter-day Saints, Brigham Young University (BYU) strives to be among the exceptional universities in the world. At BYU, we are devoted to our faith and to our students. We take an active role in the University's Mission: "To assist individuals in their quest for perfection and eternal life.” Our unique mission, deeply rooted in the Gospel of Jesus Christ, provides countless ways to serve and make an impact. This, along with our remarkable culture of belonging, weekly devotionals, and endless opportunities for learning and growth—all situated within a beautiful and historic campus—make it hard to imagine a more inspiring place to work. Brigham Young University strongly prefers to hire faithful members of The Church of Jesus Christ of Latter-day Saints. Research Project Manager (TEMPORARY) The Project Manager will oversee the planning, coordination, and execution of a multidisciplinary human subjects research study investigating dietary sulfur (sulfites and sulfates) sensitivity. This role is responsible for managing IRB compliance, participant recruitment and scheduling, biospecimen collection logistics (blood, urine, and related samples), and coordination of laboratory analyses including gene expression, metabolomics, and analytical chemistry workflows (e.g., HPLC, GC-MS). The Project Manager will serve as the central point of communication among clinical staff, laboratory personnel, and investigators, ensuring protocol adherence, data integrity, and timely completion of study milestones. Strong organizational skills, experience with human subjects research, and the ability to manage complex, cross-functional workflows are essential. What you’ll do in this position: A Project Manager in this study would be responsible for making (or guiding) several critical operational and scientific-support decisions that directly impact study quality, compliance, and timelines. Key decisions include: Protocol adherence vs. feasibility adjustments — deciding when minor deviations (e.g., timing of biospecimen collection, missed dietary restriction windows) are acceptable versus when a participant must repeat or be removed from a study arm. Dose escalation and safety thresholds — working with clinical oversight to determine whether participants can safely proceed to higher sulfite/sulfate exposure levels based on observed symptoms or biomarkers. Resource allocation and prioritization — balancing lab capacity (e.g., HPLC, GC-MS, PCR platforms) with sample throughput, deciding which analyses are prioritized if bottlenecks arise. Data quality control thresholds — determining when data (e.g., gene expression outliers, metabolomics variability, sample degradation) are acceptable, require re-analysis, or should be excluded. Vendor and supply decisions — selecting and managing suppliers for reagents, sulfite dosing materials, and collection kits, especially if substitutions are needed due to availability or stability concerns.
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Career Level
Manager
Number of Employees
501-1,000 employees