Clinical Research Associate: Data Integrity & Study Start-Up

Cone Health Medical Group; Burlington (NC); On-site; USD 52,000 - 75,000; Full time

Job summary

Cone Health Medical Group seeks a Research Associate to support investigator-led and grant-funded studies at the hospital and affiliated sites. You will assist in data collection, documentation, and study coordination to ensure robust, compliant data for conclusions.

Under supervision, you will help with screening, IRB-related submissions, and regulatory adherence, handling administrative tasks and contributing to grant applications as part of a multidisciplinary research team.

Qualifications

• Bachelor's degree with 3 years of research experience or an Associate's degree with 5 years of research experience.
• Experience supporting clinical or academic research projects.
• Knowledge of regulatory requirements and good clinical practices.

Responsibilities

• Assembles data and performs quality control checks to ensure the accuracy and reliability of research findings.
• Assists with subject recruitment, literature gathering, and IRB document submission.
• Ensures regulatory compliance and adheres to Good Clinical Practices for clinical research, maintaining HIPAA and ethical standards.
• Performs administrative and clerical responsibilities requiring analysis and knowledge of study protocols.
• Plans and conducts various activities to support research projects.
• Provides operational and clerical support for project-related activities, including editing reports and assisting with grant applications.
• Performs other duties as assigned.

Skills

Data quality checks

IRB documentation

Regulatory compliance

Study coordination

Education

Bachelor's Degree + 3 years of research experience

Associate's Degree + 5 years of research experience

Job description

Cone Health Medical Group seeks a Research Associate to support investigator-led and grant-funded studies at the hospital and affiliated sites. You will assist in data collection, documentation, and study coordination to ensure robust, compliant data for conclusions.

Under supervision, you will help with screening, IRB-related submissions, and regulatory adherence, handling administrative tasks and contributing to grant applications as part of a multidisciplinary research team.