Research Compliance Specialist

🕒 July 8

Apply Now
Find Similar Remote Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Logo of The Chicago School

The Chicago School

201 - 500 employees

Founded 1979

📚 Education

🤝 Non-profit

🏥 Healthcare

Education • Non-profit • Healthcare

The Chicago School is a nonprofit university focused on training professionals to improve the health of individuals, organizations, and communities. It offers more than 40 academic programs across bachelor’s, master’s, education specialist, and doctoral degree levels as well as certificates and continuing education. Areas of study highlighted include psychology, counseling, behavioral sciences, business, and medicine (Illinois College of Osteopathic Medicine), organized across multiple colleges such as the College of Professional Psychology and the College of Undergraduate Studies. The institution operates campuses in major U. S. metropolitan areas (Chicago, Los Angeles, Anaheim, Dallas, Washington, D. C. ) and provides online learning, career development, community-engaged centers and institutes, and student support services. The school emphasizes applied education, diversity, community impact, accreditation and regulatory compliance.

📋 Description

• provide comprehensive support for the institution’s research compliance program, including compliance monitoring and education and training • conduct compliance assessments, support audits, and partner with academic and administrative units to promote research integrity and accountability • develop and deliver human research protections training for faculty, staff, and students • create educational materials, coordinate workshops and webinars, and partner with academic units to strengthen ethical research practices throughout the institution • serve as a key resource for faculty, staff, and external partners, ensuring adherence to federal regulations, institutional policies, and best practices in human subjects research

🎯 Requirements

• Bachelor’s degree in relevant field (e.g., research compliance, public health, social sciences, etc.) • 3 years relevant program experience • Experience with human subjects research, IRB operations, research compliance, education and training • Familiarity with compliance auditing or monitoring practices • Knowledge of federal regulations governing research and institutional policies • Strong analytical, organizational, and documentation skills • Experience developing training programs or educational materials • Excellent written and verbal communication skills • Ability to manage multiple priorities and work independently • Strong interpersonal skills with a collaborative and service-oriented approach • Discretion and professionalism in handling sensitive information • Proficiency with Microsoft Office and electronic research/compliance systems • Comfortable working in a fully remote environment using tools such as Zoom

🏖️ Benefits

• generous paid time-off • medical and dental insurance coverage • life and disability insurance • retirement plan with employer contribution • multiple flexible spending accounts • tuition reimbursement

Apply Now

Similar Jobs

🕒 July 8

Lifelancer

51 - 200

💼 Consulting

🏥 Healthcare

📦 Logistics

Clinical Research Associate managing clinical research projects for Rare Diseases at Worldwide Clinical Trials. Overseeing research activities and ensuring compliance with regulatory requirements.

🇺🇸 United States – Remote

💵 $97k - $193k / year

💰 Pre Seed Round on 2022-03

⏰ Full Time

🟠 Senior

🔬 Research Analyst

🕒 July 8

Lifelancer

51 - 200

💼 Consulting

🏥 Healthcare

📦 Logistics

Senior Clinical Research Associate managing site activities in Oncology clinical studies. Collaborating with teams for effective patient data collection and compliance in the Central U.S.

🇺🇸 United States – Remote

💵 $97k - $193k / year

💰 Pre Seed Round on 2022-03

⏰ Full Time

🟠 Senior

🔬 Research Analyst

🕒 July 8

UBC

1001 - 5000

🏥 Healthcare

💼 Consulting

🧬 Biotechnology

Senior Clinical Research Associate monitoring clinical trials for UBC. Ensuring protocol adherence and managing site activities with a travel requirement in North America.

🕒 July 8

AbbVie

10,000+ employees

🏥 Healthcare

💼 Consulting

🏭 Manufacturing

Clinical Research Associate II contributing to AbbVie's pipeline through clinical research excellence. Partnering with investigators and site staff for effective clinical trial engagements.

🕒 July 7

Rho

501 - 1000

🏥 Healthcare

💼 Consulting

📦 Logistics

Clinical Research Associate at Rho driving project success through clinical monitoring and site management. Ensuring compliance with ICH Good Clinical Practices and contributing to healthcare solutions.