Open Rank Clinical Sciences Professional (Entry to Intermediate)

$47,743 - $66,088/Yr

University of Colorado - Aurora, CO

Full-time - Entry Level

Aurora, CO

Educational Services

About the position

The Open Rank Clinical Sciences Professional position at the University of Colorado Anschutz Medical Campus involves screening and enrolling patients in clinical and observational studies, primarily focused on asthma exacerbations in children. The role encompasses various responsibilities related to clinical trials, including obtaining medical histories, performing informed consent processes, and ensuring compliance with regulatory standards. This position is suitable for entry to intermediate level candidates and offers opportunities for professional growth within a dynamic research environment.

Responsibilities

• Assist with and oversee the day-to-day operations of clinical trials and studies.
• Obtain the study subject's medical history and current medication information.
• Review research protocol inclusion/exclusion criteria and confirm eligibility of subjects.
• Perform the informed consent process or ensure proper documentation of it.
• Interview prospective subjects for various research clinical trials.
• Educate potential subjects on study details through phone contacts and personal interviews.
• Schedule subject participation in research trials, coordinating necessary resources.
• Collect, code, and analyze data from research accurately and timely.
• Maintain detailed records to ensure compliance with FDA and other regulatory guidelines.
• Participate in subject recruitment efforts and pre-screening activities.
• Ensure necessary supplies and equipment for studies are in stock and functional.
• Perform study procedures such as collecting nasal swabs and obtaining lung function measurements.
• Create and resolve queries regarding data collection and study variables.
• Independently master study materials and perform study-related processes as defined in protocols.
• Assist in the coordination of multiple trials/studies and train junior team members.

Requirements

• Bachelor's degree in any field (Entry Level).
• Bachelor's degree in any field and one year of clinical research or related experience (Intermediate Level).
• Knowledge of federal regulations and Good Clinical Practice (GCP).
• Ability to communicate effectively, both in writing and orally.
• Outstanding customer service skills.
• Ability to work autonomously and under supervision.

Nice-to-haves

• Bachelor's degree in science or health-related field.
• Two years of clinical research or related experience.
• Experience with electronic data capture systems.
• Prior experience performing the Informed Consent process.
• Bilingual (English/Spanish).
• Prior experience working in an emergency/outpatient setting.

Benefits

• 401(a) retirement plan with employer contributions.
• Dental insurance.
• Disability insurance.
• Health insurance.
• Paid time off including vacation and sick days.