Associate Clinical Research Coordinator

University-of-North-Carolina-At-Chapel-Hil; Eastowne (NC); On-site; USD 52,000 - 70,000; Full time

Benefits offered by this job

Comprehensive benefits package

Job summary

University of North Carolina at Chapel Hill is seeking an Associate Clinical Research Coordinator in the Department of Medicine, Division of Pulmonary Diseases and Critical Care Medicine. The role supports execution of clinical research protocols, regulatory tasks, recruitment, informed consent, and data management for multiple studies at the Chapel Hill campus.

This on-site position may include evening hours and requires a Bachelor’s degree or equivalent, with knowledge of Good Clinical

Qualifications

• Knowledge of Good Clinical Practice (GCP) and regulatory standards.
• Experience coordinating IRB submissions and study documents.
• Ability to collect, manage and report clinical data accurately.

Responsibilities

• Execute and monitor clinical research protocols across studies.
• Assist with recruitment, informed consent, and participant scheduling.
• Maintain regulatory documentation and ensure data integrity and compliance.

Skills

Clinical research

IRB submissions

Education

Bachelor’s degree

Job description

Full-time/Part-time Permanent/Time-Limited

Full-time/Part-time Permanent/Time-Limited Full-Time Permanent

If time-limited, estimated duration of appointment

Hours per week 40

Work Schedule

Work Location

Work Location 800 Eastowne Dr (office); 100 Eastowne Dr (clinic), Chapel Hill, NC

This position is not eligible for H-1B sponsorship.

One of the best college towns and best places to live in the United States, Chapel Hill has diverse social, cultural, recreation and professional opportunities that span the campus and community.

University employees can choose from a wide range of professional training opportunities for career growth, skill development and lifelong learning and enjoy exclusive perks for numerous retail, restaurant and performing arts discounts, savings on local child care centers and special rates on select campus events. UNC -Chapel Hill offers full-time employees a comprehensive benefits package , paid leave, and a variety of health, life and retirement plans and additional programs that support a healthy work/life balance.

Primary Purpose of Organizational Unit

Our mission is to improve the health and well-being of North Carolinians and others whom we serve. We accomplish this by providing leadership and excellence in the interrelated areas of patient care, education and research.

Patient care

We promote health and provide superb clinical care while maintaining our strong tradition of reaching underserved populations and reducing health disparities across North Carolina and beyond.

Education

We prepare tomorrow`s healthcare professionals and biomedical researchers from all backgrounds by facilitating learning within innovative and integrated curricula and team-oriented interprofessional education to ensure a highly skilled workforce.

Research

We develop and support a rich array of outstanding health sciences research programs, centers and resources. We provide infrastructure and opportunities for collaboration among disciplines throughout and beyond our university to support outstanding research. We foster programs in the areas of basic, translational, mechanistic and population research.

Position Summary

This position will serve as an Associate Clinical Research Coordinator within the Department of Medicine, Division of Pulmonary Diseases and Critical Care Medicine. The Associate Clinical Research Coordinator is responsible for the execution of clinical research protocols, including leading efforts in gathering, compiling, and reporting data for a variety of research studies. This position provides support to the research efforts in the Division. The position will participate in all aspects of clinical trial conduct within the Division, including regulatory, recruitment, informed consent, study procedures, data, documentation and database management. This position will support the Clinical Research Coordinators to track progress, evaluate protocols, and provide support to other research personnel as necessary to ensure the successful execution of all clinical trials.

Minimum Education and Experience Requirements

Bachelor’s degree; or equivalent combination of training and experience. All degrees must be received from appropriately accredited institutions.

Management Preferences

Knowledge of and relevant experience in clinical research. An understanding of Good Clinical Practice standards and experience with regulatory & IRB submissions will be highly valued. The ability to effectively interact with research staff and colleagues to validate and/or redirect research based on documented results. Ability to make recommendations in the area of research or program policy through effective communication.

Special Physical/Mental Requirements

Not Applicable.

Campus Security Authority Responsibilities

Not Applicable.

Position/Schedule Requirements

Position/Schedule Requirements Clinic – UNCH or ACC, Evening work occasionally, Exposure to Bloodborne Pathogens, Exposure to Hazardous Materials, Laboratory, Overtime occasionally, Valid NC Driver’s License

Equal Opportunity Employer Statement

The University is an equal opportunity employer and welcomes all to apply without regard to age, color, gender, gender expression, gender identity, genetic information, national origin, race, religion, sex, or sexual orientation. We encourage all qualified applicants to apply, including protected veterans and individuals with disabilities.

Required Documents

• Curriculum Vitae / Resume
• Cover Letter
• List of References

Optional Documents

Posting Supplemental Questions

Required fields are indicated with an asterisk (*).

• * Please select the response below that best describes your experience/education for the Social/Clinical Research Assistant position.
  • Bachelor's, Master's, and/or Doctorate in any field.
  • Associate's in any field and at least 2 years of experience.
  • Combination of post-high school education and experience to equal at least 4 years of related experience (ex: 1 year towards a degree and 3 years of experience).
  • High School diploma/GED and at least 4 years of related experience.
  • Did not complete high school but have a combination of high school education and experience to equal 8 years. (ex. 3 years of high school and 5 years of experience).
  • None of the above
• * Do you have previous experience working with industry sponsored clinical trials?
  • Yes
  • No