Bon Secours Health System·Richmond, Virginia
Implement and manage active clinical research programs, including trial start-up and coordination with legal, finance, and compliance departments. Responsibilities include handling patient consents, managing regulatory IRB submissions, and tracking safety reports and annual reviews.
Thank you for considering a career at Bon Secours!
Scheduled Weekly Hours: 40
Work Shift: Days (United States of America)
To implement and manage aspects of all active clinical research programs and to assist in other activities as assigned by investigator providers related to these programs with responsibilities to include, but not limited to: interacting with BSHSI legal, finance, compliance, and other departments as appropriate to help start up new clinical trials. Handle consents and agreements, capture patient data and enter it into confidential data management systems provided by industry sponsors, handle regulatory (IRB) submissions for new clinical trials, submit Serious Adverse Event (SAE) information to IRBs, handle amendments, manage safety reports and submit to IRBs as appropriate, track annual review dates and submit continuing reviews, and assist with departmental needs as requested in a back-up capacity.
$26.82
$41.57
Bon Secours is an equal opportunity employer.
As a Bon Secours [https://careers.bonsecours.com/us/en/life-at-bon-secours?utm_source=job_description] associate, you’re part of a Mission that matters. We support your well-being – personally and professionally. Our benefits are built to grow with you and meet your unique needs, every step of the way.
may vary based on the market and employment status.
It is our policy to abide by all Federal and State laws, as well as, the requirements of 41 CFR 60-1.4(a), 60-300.5(a) and 60-741.5(a). Accordingly, all applicants will receive consideration for employment without regard to race, color, national origin, religion, sex, sexual orientation, gender identity, age, genetic information, or protected veteran status, and will not be discriminated against on the basis of disability. If you’d like to view a copy of the affirmative action plan or policy statement for Mercy Health– Youngstown, Ohio or Bon Secours – Franklin, Virginia; Petersburg, Virginia; and Emporia, Virginia, which are Affirmative Action and Equal Opportunity Employer, please email recruitment@mercy.com [recruitment@mercy.com]. If you are an individual with a disability and would like to request a reasonable accommodation as part of the employment selection process, please contact The Talent Acquisition Team at recruitment@mercy.com [recruitment@mercy.com].
Market context
Clinical Research Coordinator roles in Virginia often draw steady interest from hospitals, cancer centers, and academic research programs, especially when the work supports oncology studies and regulatory compliance. This type of role is competitive because employers typically want a health or life sciences degree, hands-on research or regulatory experience, and familiarity with FDA, ICH-GCP, and IRB requirements. Review the AI-summarized requirements and benefits here to save time, then tailor your application to show direct protocol, consent, and regulatory coordination experience.
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