Founded in 1946, the Oklahoma Medical Research Foundation (OMRF) is among the nations oldest, most respected independent, nonprofit biomedical research institutes. OMRF is dedicated to understanding and developing more effective treatments for human diseases, focusing on critical research areas such as Alzheimers disease, cancer, lupus, Multiple Sclerosis, and cardiovascular disease. OMRF follows an innovative cross-disciplinary approach to medical research and ranks among the nations leaders in patents per scientist.

Located in Oklahoma City, a city that offers a dynamic and flourishing downtown area, with low cost of living, short commute times and a diversified economy, OMRF has been voted one of the Top Workplaces since the inception of the award. This achievement has been accomplished thanks to OMRF individuals who share a unified understanding that our excellence can only be fully realized with a commitment to diversity, equity, and inclusion. Successful candidates will demonstrate commitment to these values.

OMRF is an Equal Opportunity/Affirmative Action/Veterans Employer. All qualified applicants will receive consideration for employment without regard to gender, sexual orientation, gender identity, race, color, national origin, age, religion, disability, veteran status, or any other legally protected characteristic.

Support Clinical Research Coordinators (CRC) in conduct of clinical research activities.
Prep for research visits by gathering all relevant documents and supplies.
Assist clinician investigators in the examination process.
Administer patient questionnaires, both paper and electronic.
Maintain patient and research records and adhere to the Health Insurance Portability and Accountability Act (HIPAA).
Clean equipment and instruments and dispose of contaminated supplies.
Assists with approved research subject recruitment, retention and communication.
Maintain necessary records and complete paperwork.
Perform accurate, legal, and ethical documentation at all times.
Input patient/participant data into research databases.

High school diploma or GED and 1 year of relevant experience or combination of education and experience.

Must demonstrate strong organizational skills. Must be detail oriented, flexible, adaptive, and have excellent oral and written communication skills. Must have the ability to deal professionally with diverse personalities and cultures in stressful and difficult situations. Ability to work under strict deadlines, maintain confidential information and keep up-to-date technically. Must have the ability to multi-task, work independently and as a team player.

Previous exposure to a research environment
Bilingual (English/Spanish)

Experience with data entry, managing patient files and records, and medical terminology

Typically, Monday through Friday, 8:30am to 5:00pm (hours may vary with advanced notice depending on workload).