Clinical Research Associate

University of New Mexico•Albuquerque, NM

10d•$5,845 - $8,367•Onsite

About The Position

The Division of Endocrinology, within the Department of Internal Medicine, is seeking a Clinical Research Associate. This position will manage quality controls and the execution of clinical protocol and data management for two clinical trials, ensuring compliance with all regulatory and contractual requirements. They will establish and maintain sound clinical and data collection practices to ensure validity of studies. This position will monitor the conduct and progress of the studies to ensure compliance with established protocols, appropriate research methodology, and study timelines. They will participate in protocol development, site/investigator selection, study initiation and termination activities. In addition, they will develop and complete mid-year and final study reports. The Department of Internal Medicine is a large, progressive department with a diverse staff working in dedicated teams to provide quality work in an organized, effective, and efficient manner through innovation, training, and education. Through our collaborative work effort, we support the faculty and enhance the missions of the department, school, Health Sciences Center, and University.

Requirements

Bachelor's degree
At least 5 years of experience directly related to the duties and responsibilities specified.
Completed degree(s) from an accredited institution that are above the minimum education requirement may be substituted for experience on a year for year basis.
Successful candidate must submit to post-offer, pre-employment physical examination and medical history check.
Background Check Required

Nice To Haves

Experience in developing, maintaining, and managing databases and tracking systems
Experience in managing study data reporting and measurement
High-level of experience in leading regulatory support for two studies with multiple IRBs
Experience in the Project Management of research activities
Possession of or ability to obtain certification as a Clinical Associate

Responsibilities

Manage quality controls and the execution of clinical protocol and data management for two clinical trials, ensuring compliance with all regulatory and contractual requirements.
Establish and maintain sound clinical and data collection practices to ensure validity of studies.
Monitor the conduct and progress of the studies to ensure compliance with established protocols, appropriate research methodology, and study timelines.
Participate in protocol development, site/investigator selection, study initiation and termination activities.
Develop and complete mid-year and final study reports.