Study Coordinator
Study Coordinator
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$ 53203 - 60222
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
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
At UCCS our employees are our most valued asset. Were proud to offer:
Generous Time Off: Enjoy 22 vacation days 10 sick days paid parental leave 13 recognized holidays and provisions for bereavement jury duty and FAMLI Leave. - Robust Health Coverage: Our comprehensive medical plans cover preventative care at no cost including a yearly mental health visit. Plus benefit from affordable dental vision plans and competitive prescription drug prices.
- Financial & Retirement Benefits: Take advantage of our health savings flexible spending accounts and life and disability insurance. Plan for your future with our retirement options.
- Further Your Education: Avail nine waived credits per academic year for courses at any CU campus. We invest in your educational and professional growth.
- Wellness & More: From wellness programs aimed at achieving your best self to various additional benefits through CU Advantage we prioritize well-being and holistic development.
- Want to know your total compensation Use ourcalculator to get the complete picture.
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:
- Be primary contact for potential participants. Oversee promotion screening randomization and monthly survey emails.
- Maintain database of potential and recruited participants.
- Maintain detailed records of study to ensure compliance with DoD and UCCS IRB.
- Oversee actigraphy watches for mom and baby maintain tracking shipping/receipt of study materials and database.
- Oversee blood collection kits: shipping supplies and return.
- Oversee shipment of assigned bassinet to participant. Ensure proper return to SB when participant is finished with study.
- Communicate with other research sites and personnel.
- Assist Dr. Okun with IRB materials.
- Manage research assistant share duties.
Tentative Search Timeline
- Priority will be given to applications submitted by: June 8 2025.
- Potential interview dates: June 8-June 12 2025.
- Potential start date: June 22 2025.
Required Experience:
IC
Employment Type
Full-Time
