Clinical Research Monitor (Hybrid)

Welcome to Virginia Commonwealth University (VCU) ... a world UNLIKE
any other!

At VCU, we are UNCOMMON and UNLIKE any other university. A premier, urban, public research university nationally recognized as one of the best employers in Virginia. We know that the unique backgrounds and life experiences of the Virginia Commonwealth University (VCU) community are what drive the university forward. Together, we’re forging a future that is built by us. Here, artists and engineers, doctors and designers come together to re-imagine the human experience and tackle the problems of tomorrow.

VCU is a great place to work. It’s a place of opportunity where your success is supported and your career can thrive. VCU offers employees a generous leave package, career paths for advancement, competitive pay, and an opportunity to do mission-driven work.

VCU's Office of the Vice President for Research and Innovation and its Research Strategy and Regulatory Affairs Office invite all interested candidates to apply for our Clinical Research Monitor position. This is a hybrid role.

Our impact is measured one student and patient at a time. VCU’s unequaled combination of excellence, research and creativity makes success possible for every one of our 300,000+ “RAMily” members. And that makes us one of the most innovative universities in the country.

All full-time staff are eligible for our generous benefits package that includes choices for health, vision, and dental coverage, life-insurance, short and long-term disability coverage, retirement planning, tax-deferred annuity and cash match programs, flexible spending accounts, tuition benefits, significant paid-time off,12 paid holidays, and more. Explore our benefits further here: https://hr.vcu.edu/current-employees/benefits/

Primary Purpose and General Responsibilities:

Perform randomly selected monitoring visits and for cause auditing of FDA regulated clinical trials
Deliver monitoring confirmation letters and monitoring reports to study teams
Work with study teams on monitoring findings by identifying root causes of findings and then addressing through education to study teams and help with internal process improvement
Identify trends seen across monitoring of clinical trials; identify where there is gaps in resources or support
Provide assistance, training and education to study teams in utilizing Veeva SiteVault and Veeva eTMF
Other regulatory-related tasks as needed