Days

UHS•Amarillo, TX

1d•Onsite

About The Position

Northwest Texas Healthcare System is a 495 bed system serving the city of Amarillo and the surrounding region. We offer the ideal combination of traditional values and the most advanced technologies in healthcare, plus the conveniences of big city living in a friendly, smaller-town atmosphere. From the beauty of Palo Duro Canyon and great recreational facilities, to our quality educational system, Amarillo is a great place to live and work. A hospital is only as good as its caregivers. That's why we're looking for health professionals who are dedicated and passionate about their work. We're looking for employees who can add to our culture of exemplary patient care and personal excellence. We're looking for exceptional professionals who share our vision and values. Visit us online at: https://www.nwths.com/careers POSITION SUMMARY: Reporting to the Director of Trauma Services, the Lead Clinical Research Coordinator supports the planning, coordination, execution, and documentation of research activities that involve statistical analysis, study design support, data management, and regulatory compliance. This position serves as a key operational link between investigators, research staff, data analysts, and other stakeholders to ensure that research projects are conducted accurately, efficiently, and in accordance with approved protocols, institutional policies, and applicable regulations. The role is responsible for assisting with the collection, organization, cleaning, tracking, and reporting of research data, as well as supporting the biostatistical needs of ongoing studies through coordination, quality control, and effective communication. This position requires a high degree of accuracy, professionalism, confidentiality, and attention to detail. The Lead Clinical Research Coordinator must be able to manage multiple priorities, maintain organized records, support timelines for active studies, and collaborate effectively with multidisciplinary teams. The role also requires familiarity with research processes, data integrity standards, and basic statistical concepts in order to support both routine and complex research activities.

Requirements

Demonstrated knowledge of research coordination principles, data management practices, and statistical analysis principles
Advanced understanding of how to support study workflows from project initiation through completion, including documentation, data review, and communication with project stakeholders
Advanced analytical ability, including ability to recognize data inconsistencies, identify missing or incomplete information, and contribute to the resolution of data-related issues
Ability to understand study protocols and data collection procedures
Excellent written and verbal communication abilities
Capacity to successfully work collaboratively in a team-oriented research environment
Demonstrated ability to self-initiate work and work individually
Advanced understanding of managing confidential and sensitive information appropriately
Advanced proficiency with technology such as Microsoft Suite, database or research systems, and statistical software
Demonstrated commitment to Service Excellence standards
Bachelor’s Degree in public health, statistics, biostatistics, health sciences, biological sciences, or a related field is required.
Equivalent combinations of education and experience may be considered in lieu of a degree, depending on the needs of the department and organization.
At least one year of successful research, clinical or academic setting experience strongly preferred.

Responsibilities

Support the planning, coordination, execution, and documentation of research activities that involve statistical analysis, study design support, data management, and regulatory compliance.
Serve as a key operational link between investigators, research staff, data analysts, and other stakeholders to ensure that research projects are conducted accurately, efficiently, and in accordance with approved protocols, institutional policies, and applicable regulations.
Assist with the collection, organization, cleaning, tracking, and reporting of research data.
Support the biostatistical needs of ongoing studies through coordination, quality control, and effective communication.
Manage multiple priorities, maintain organized records, and support timelines for active studies.
Collaborate effectively with multidisciplinary teams.
Organize and present data and findings to audiences of varying sizes and populations.
Maintain accurate records.
Adapt to changing priorities and deadlines.