Coord,Research

University of New Mexico•Albuquerque, NM

1d•$20 - $27•Onsite

About The Position

The Department of Emergency Medicine is seeking to hire three motivated professionals to serve as the Research Coordinators to support and coordinate enrollment for clinical research studies. This individual will be responsible for working with a diverse team of clinical investigators and research staff to coordinate currently active research studies. Primary duties include research study subject enrollment including data and research specimen collection. Oversee student employees in screening and data entry and data quality assurance tasks. Coordinates, plans and executes study promotional activities to keep clinical staff informed about active research studies. Additional responsibilities include site investigative file maintenance, reporting of protocol of safety information to the institutional review board (IRB) as needed and regular communication with the research team and clinical trial sponsors and their representatives. This position requires applicants to work in the emergency department. Hence, applicants must be able to collect and prepare data and research specimens in accordance with protocols, maintain regulatory binders, and supervise the process of data entry and quality assurance. This position may require scheduling evening and weekend work hours in order to meet enrollment demands.

Requirements

Bachelor's degree
At least 1 year of experience directly related to the duties and responsibilities specified.
Ability to collect and prepare data and research specimens in accordance with protocols.
Ability to maintain regulatory binders.
Ability to supervise the process of data entry and quality assurance.

Nice To Haves

Experience with Microsoft Office products including spreadsheets (Word, PowerPoint, Excel)
Experience delivering oral presentations to small groups
Completion of a Human Research Protections (HRP) Training and Good Clinical Practices curriculum or program
Medical experience or current license (EMT, RN, etc.) or experience working with Protected Health Information (PHI)
Research experience including the use of data collection software (REDCap, OpenClinica, etc.)
Experience maintaining and updating clinical study binders
IRB and grant submission experience
Basic understanding of research study design and statistics

Responsibilities

Support and coordinate enrollment for clinical research studies.
Work with a diverse team of clinical investigators and research staff to coordinate currently active research studies.
Perform research study subject enrollment, including data and research specimen collection.
Oversee student employees in screening, data entry, and data quality assurance tasks.
Coordinate, plan, and execute study promotional activities to keep clinical staff informed about active research studies.
Maintain site investigative files.
Report protocol of safety information to the institutional review board (IRB) as needed.
Communicate regularly with the research team and clinical trial sponsors and their representatives.
Collect and prepare data and research specimens in accordance with protocols.
Maintain regulatory binders.
Supervise the process of data entry and quality assurance.