Clinical Research Coordinator (Open Rank: Entry – Senior)

at  University of Colorado

JOB SUMMARY:

The Department of Neurology has an opening for a motivated full-time Research Services Professional (clinical research coordinator) to coordinate human subjects research studies. Neurology’s clinical research includes over 300 human subject’s research studies: Actively Enrolling Studies (cuanschutz.edu). The successful applicant will be conducting research with the oversight of the Principal Investigator (PI), who is a clinical research scientist.

PREFERRED QUALIFICATIONS:

• Bachelor’s degree in science or health-related field.
• One (1) to three (3) years of clinical research or related experience.
• Experience with electronic data capture systems (e.g., EMR or EHR and data management systems).
• Experience performing ECGs, phlebotomy, and/or vital signs.
• Experience working with patients with Neurological conditions or Neuroscience experience.
• Bilingual in Spanish.
• SOCRA or ACRP clinical research professional certification (or other relevant certification).

KNOWLEDGE, SKILLS, AND ABILITIES:

• Knowledge and understanding of federal regulations and Good Clinical Practice (GCP).
• Ability to communicate effectively, both in writing and orally.
• Ability to establish and maintain effective working relationships with employees at all levels throughout the institution.
• Outstanding customer service skills.
• Demonstrated commitment and leadership ability to advance diversity and inclusion.
• Knowledge of basic human anatomy, physiology, and medical terminology.
• Ability to interpret and master complex research protocol information.
• Ability to respect patient rights and put patient safety first, excellent patient rapport.
• Empathetic to patients with chronic illnesses.
• Great attention to detail and quality.
• Ability to work with colleagues and patients in a confidential and professional manner.
• Ability to follow and execute a study protocol and proactively prevent deviations.
• Ability to follow direction of the PI and direct supervisor, follow all department SOPs and department policies, and follow all clinical research regulations or guidelines.

• Overseeing and supporting assigned research studies (which may include drug or device studies) as well as participating as a backup coordinator on other studies.
• Consenting clinical research participants.
• Direct participant contact: obtaining study data and working with participants.
• Data entry and other administrative duties such as scheduling.
• This position will collaborate with study colleagues at all levels of the organization.
• We are seeking an individual who is collaborative, communicative, caring, detail oriented and organized, proactive, able to think critically, focused on quality, dedicated to personal growth, and highly motivated in all areas of study coordination.