drjobs Study Coordinator

Study Coordinator

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1 Vacancy
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Job Location drjobs

Colorado Springs, CO - USA

Yearly Salary drjobs

$ 53203 - 60222

Vacancy

1 Vacancy

Job Description

Applicants must meet minimum qualifications at the time of hire.

  • A bachelors degree in health related field is required. A combination of education and related clinical research experience may be substituted for the bachelors degree.
  • Applicants must have at least 2 years clinical research experience.
  • A masters degree in science or health related field is preferred.
  • Excellent candidate will have 3 years of clinical research or related experience.
  • Experience with actigraphy is a plus.
  • Experience with Mircrosoft Excel Word SPSS is highly desired.

Study Coordinator

BioFrontiers Center

Elevate Your Career at UCCS: Innovate Inspire and Impact in the Rockies!

Who We Are

The University of Colorado Colorado Springs (UCCS) is a premier educational institution that prides itself on academic excellence research and community engagement and is actively seeking a Study Coordinator to join our team! UCCS offers a diverse and inclusive learning environment that fosters innovation growth and the holistic development of its students.

At the base of the Rocky MountainsColorado Springs is captivated by its stunning landscapes making it a paradise for nature lovers. This city is more than its scenerya mosaic of history arts and a vibrant tech scene. We invite you to join a community that cherishes outdoor adventure as much as forward-thinking growth an exceptional setting for both career and lifestyle.

Pay Range: $53203-$60222 annually. Compensation will be commensurate upon experience and qualifications. This position is an Exempt from theFair Labor Standards Act (FLSA) overtime provisions.

Work Location: On-site

Benefits at a Glance

At UCCS our employees are our most valued asset. Were proud to offer:

Summary

This individual will work closely with Dr. Okun to ensure the execution of the study especially the shipment of bassinets blood collection kits and actigraphy. This person will oversee proper dissemination of online survey links for proper data collection and that data entry is appropriately managed collected and entered. This person will be responsible for recruitment and participant management. The study coordinator will assist with and oversee the day-to-day operation of the clinical trial. This position will obtain study subjects demographic information reviews research protocal inclusion/exclusion criteria and confirms eligibility of subject to participate in clinical trial. The study coordinator ensures that the informed consent process has occurred is properly documented and that informed consent form documents are filled as required. The position will also collect code and analyze data obtained from research in an accurate and timely manner.

The funding for this position is expected to last until 6/14/2028.

Essential Functions

The duties and responsibilities of the position include but are not limited to:

Tentative Search Timeline


Required Experience:

IC

Employment Type

Full-Time

About Company

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