Clinical Research Specialist: Data Integrity & Compliance

Cone Health; Burlington (NC); On-site; USD 45,000 - 65,000; Full time

Job summary

Cone Health is seeking a Research Associate to support principal investigators in grant-funded and industry-sponsored clinical research conducted on-site at the hospital and affiliated sites. You will assist in planning, preparing, and conducting studies to ensure robust and valid data are gathered.

Under supervision, you will help with literature reviews, IRB submissions, and regulatory compliance, while collaborating with study coordinators, participants, and other research professionals to

Qualifications

• Bachelor's degree or higher required with relevant research experience.
• Experience in clinical or grant-funded research is preferred.
• Knowledge of regulatory requirements (IRB, HIPAA) and good clinical practices.

Responsibilities

• Assembles data and performs quality control checks to ensure accuracy and reliability of findings.
• Contributes to early-stage activities for research projects, including recruitment and literature gathering.
• Ensures regulatory compliance and adheres to GCP, HIPAA and ethics standards.
• Performs administrative tasks requiring analysis and knowledge of study protocols.
• Plans, prepares, implements and conducts various activities to support research projects.
• Provides operational and clerical support for project-related tasks.

Skills

Research experience

Data quality checks

Regulatory compliance

Administrative support

IRB coordination

Education

Bachelor's degree

Associate's degree

Tools

Microsoft Office

Job description

Cone Health is seeking a Research Associate to support principal investigators in grant-funded and industry-sponsored clinical research conducted on-site at the hospital and affiliated sites. You will assist in planning, preparing, and conducting studies to ensure robust and valid data are gathered.

Under supervision, you will help with literature reviews, IRB submissions, and regulatory compliance, while collaborating with study coordinators, participants, and other research professionals to