Clinical Research Coordinator · On-site in Orem · Lead or assistant level View

You'll work across every part of trial operations at a fast-growing site, with close involvement in each study from startup through close-out.

We're hiring at one of two levels, depending on experience. A lead coordinator takes ownership of site operations. An assistant coordinator has some research experience and wants to grow.

• Study startup: regulatory submissions, site initiation prep, and document organization
• Regulatory upkeep: IRB submissions, amendments, continuing reviews, and TMF/eReg
• Recruitment and pre-screening: phone screens, chart review, and coordination with the PI
• Scheduling and coordinating study visits
• Source documentation, eSource/eReg workflows, data entry, and query resolution
• Documenting deviations, AEs/SAEs, and other reportables per SOPs
• Working with sponsors, CROs, and monitors, and supporting audits and inspections
• Participant procedures as delegated: consent support, vitals, ECGs, blood draws, and sample processing and shipping

• About 5+ years of clinical research experience
• Prior work as a lead or senior coordinator
• Ideally 2+ years in psychiatry or CNS trials
• Strong grasp of GCP, regulatory processes, and site operations
• Able to work independently and mentor junior staff

• Some clinical research experience (site, academic, or CRO)
• Familiarity with basic research workflows and GCP
• Strong organization and eagerness to learn
• Interest in psychiatric and psychedelic research

• Experience with eRegulatory and eSource/CTMS platforms, especially CRIO
• Clear communication and attention to detail
• A respectful, participant-centered approach
• Comfort in a growing, hands-on environment

• Competitive salary based on experience and level
• Health, dental, and vision insurance
• Paid time off