Open Rank Clinical Research Coordinator (Entry – Senior)

The University of Colorado is hiring an Open Rank Clinical Research Coordinator to support research activities in Dr. Neda Rasouli’s Research Program. The role coordinates clinical trials, recruits and supports study participants, performs protocol-defined clinical procedures, manages study data and regulatory records, and contributes to safety reporting and staff training.

Responsibilities

Assist with and oversee day-to-day operations for multiple clinical trials, acting as the Primary Coordinator to ensure all study activities align with the established protocol

Participate and lead recruitment efforts by interviewing prospective subjects, reviewing medical histories against inclusion/exclusion criteria, and confirming final eligibility

Execute and document the informed consent process, ensuring all participants are fully educated on study details and that legal documentation is filed per regulatory standards

Perform study-related procedures, assessments, and drug administrations as defined in the research protocol and in compliance with governing bodies

Manage the logistics of subject participation, including the coordination of clinic space and multidisciplinary support (Radiology, Pharmacy, Lab, and PIs)

Perform technical clinical tasks including phlebotomy (venipuncture), specimen processing/shipping, EKGs, and monitoring vital signs

Abstract, code, and record patient data into Case Report Forms (CRFs) and clinical trial databases with a focus on accuracy and timely entry

Maintain meticulous study records to ensure strict adherence to FDA guidelines, Good Clinical Practice (GCP), and hospital Standard Operating Procedures (SOPs)

Promptly alert Principal Investigators, sponsors, and the FDA regarding Serious Adverse Events (SAEs) to ensure patient safety and data integrity

Assist in the creation of new clinical processes and quality initiatives while training junior staff members on study protocols

Preferred

Three (3) years clinical research or related experience

Three (3) years clinical research or related experience.

Benefits

Medical: Multiple plan options

Dental: Multiple plan options

Additional Insurance: Disability, Life, Vision

Retirement 401(a) Plan: Employer contributes 10% of your gross pay

Vacation Days: 22/year (maximum accrual 352 hours)

Sick Days: 15/year (unlimited maximum accrual)

Holiday Days: 15/year

Tuition Benefit: Employees have access to this benefit on all CU campuses

ECO Pass: Reduced rate RTD Bus and light rail service

This position may be eligible for overtime compensation, depending on the level.

Company

Public research university with four Colorado campuses

Denver, Colorado, USA

https://www.cu.edu/

Founded in 1876

10001+ employees

Qualifications

Bachelor's degree in science or health related field

One (1) year clinical research or related experience

Two (2) years clinical research or related experience

A combination of education and related technical/military/paraprofessional experience may be substituted for a bachelor's degree on a year for year basis

Applicants must be legally authorized to work in the United States without requiring sponsorship. We are unable to provide work visa sponsorship or employment authorization for this position now or in the future

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

Knowledge of basic human anatomy, physiology, and medical terminology

An understanding of genetics and molecular genetics

Ability to interpret and master complex research protocol information

Excellence with computer skills with Microsoft Office, including Word, Excel, PowerPoint and Outlook

Knowledge of the research process, e.g., research protocols, surveys

Three (3) years clinical research or related experience

One (1) year clinical research or related experience.

Two (2) years clinical research or related experience.

A combination of education and related technical/military/paraprofessional experience may be substituted for a bachelor’s degree on a year for year basis.

Required skills

Human Anatomy, Physiology, Medical Terminology, Genetics, Molecular Genetics, Clinical Research, Research Protocols, Microsoft Office, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Outlook

Preferred skills

Three (3) years clinical research or related experience

Experience

1-2 years