Clinical Sciences Professional (Open Rank)

University of Colorado•Aurora, CO

2d•Onsite

About The Position

Established in 2010, the Anna and John J. Sie Center for Down Syndrome at Children’s Hospital Colorado is one of the leading Down syndrome clinics in the United States. Our world-renowned team of experts provides medical, educational, and therapeutic care that helps children and adolescents with Down syndrome thrive. Through close partnership and collaboration with the Global Down Syndrome Foundation and Linda Crnic Research Institute, the Sie Center is a model for Down syndrome care, combining excellence in clinical care, research, community engagement, advocacy, and education. In the first 14 years, the Sie Center has served over 2,500 patients from 32 states, Puerto Rico, and 11 countries. Our pediatric specialists work together to provide the best possible collaborative care for children with Down syndrome using a multidisciplinary team-based approach. Our services include evaluation, consultation, and therapies for infants, children, teens, and young adults through the age of 22.

Requirements

Bachelor’s degree in any field.
One (1) year of clinical research or related experience (Intermediate Level).
Two (2) years of clinical research or related experience (Senior Level).
Applicants must meet minimum qualifications at the time of hire.
Must successfully pass a drug test through Children’s Hospital Colorado
Must be willing and able to pass a national criminal background check

Nice To Haves

Bachelor’s degree in science or health related field.
Three (3) years of clinical research or related experience.
Experience with electronic data capture systems (e.g., EMR or EHR and data management systems).
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.
Knowledge of basic human anatomy, physiology, and medical terminology.
Ability to interpret and master complex research protocol information.
Ability to multitask and meet deadlines.
Ability to proactively identify and solve problems.
Demonstrated initiative and strong follow-through skills.

Responsibilities

Act as a Primary Coordinator on multiple trials/studies, managing the day-to-day operations.
Develops protocol-specific source documents and organizes and prepares research materials for research study visits.
Lead participant recruitment, communication, and scheduling.
Administer developmental assessments and study interviews.
Responsible for data management for all clinical trial data. Collect, code, and analyze data obtained from research in an accurate and timely manner.
Reviews and resolves data discrepancies in data management systems.
Accurately and timely enters clinical trials data into centralized data management systems, ensures data quality, and reviews participant records for completeness, accuracy, and quality.