Site Director - Clinical Research - Las Vegas, NV

What You’ll Do: Supervise Clinical Research Staff and oversee daily site activities, including protocol feasibility, budgets, and study participant management Own study financials — budget oversight, income/expense tracking, and compliance reporting to leadership Recruit, train, and mentor research staff; set performance goals and lead development of SOPs and operational tools Drive quality control initiatives, partner with leadership and HR on staffing issues, and conduct annual performance reviews

What You Bring: Bachelor's degree Site‑level clinical trial experience 2-5 years of site‑level management experience Master's degree, RN, NP, or PA-C preferred SoCRA CCRP certification a plus

Why You’ll Love It Here: Full medical, dental, and vision coverage Generous PTO, holidays, and a floating holiday 401k with employer match Tax‑free tuition and student loan repayment assistance Paid maternity and parental leave No on‑call responsibilities — when you're home, you're off The IMA Group is an affirmative Action/

Equal Opportunity Employer: Our Government Services Division supports local, state, and federal agencies and delivers professional and objective medical and psychological examinations as well as ancillary services. Our Payer Services Division meets the evaluation and screening needs of Carriers, TPAs, Public Entities and Employers and includes behavioral health and physical medicine specialty services, working with a wide range of organizations within the workers' compensation, disability, liability, and auto markets. Our Clinical Research Division performs all types of Phase II‑IV clinical trials in multiple therapeutic areas through a flexible nationwide network of site locations and virtual capabilities.#LI-RC1 #LI-ONSITE