Clinical Research Coordinator II (Full-Time)

Colorado ENT and Allergy•Colorado Springs, CO

7d•$23 - $28•Onsite

About The Position

Colorado ENT & Allergy is the premier (and the largest) ENT practice in the state of Colorado. We are dedicated to providing the most exceptional ear, nose, throat, allergy, asthma and sleep medicine care to our patients. To accomplish this goal, we continuously promote advancements in clinical practice through clinical trials and the utilization of state-of-the-art technology which benefits both our patients and employees. We are seeking a Highly Skilled and Experienced Clinical Research Coordinator II to join our team, Full-Time

Requirements

Candidates with a Bachelor's degree in a scientific or health related program, preferred.
Preferred candidates will have three or more years as a clinical research professional (certification as a CCRC is desired).
Knowledge of medical terminology, clinical medicine, clinical trials and GCP concepts.
Detail-oriented and meticulous in all aspects of work.
Strong follow-through skills and ability to proactively identify and solve problems; demonstrated initiative is imperative.
Must have professional demeanor and strong communication skills with the public as well as physicians/researchers.
Ability to work well independently as well as in a team environment.
Strong interpersonal, customer service, and multi-tasking skills are critical.
Must be proficient in Microsoft Office Word and Excel, electronic health systems and databases used in a research environment or have a willingness to learn and demonstrate proficiency.
Ability to be flexible, organized, detail-oriented and tenacious in follow-through.
Possess the ability to work well under pressure, multi-task and manage deadlines.
Knowledge of GCP, federal, state, and local regulations, including HIPAA policies and procedures.

Nice To Haves

Preferred candidates will have three or more years as a clinical research professional (certification as a CCRC is desired).

Responsibilities

Reviews and develops a thorough understanding of the protocol, e.g., study proceedings and timelines, inclusion and exclusion criteria, confidentiality, privacy protections.
Screen patients for eligibility using protocol specific inclusion and exclusion criteria, documenting each potential participant's eligibility or exclusion.
Collects data as required by the protocol. Assures timely completion of Case Report Forms. Maintains study timelines.
Completes patient study visits and documentation and maintains study files in accordance with sponsor requirements and policies and procedures including, but not limited to, consent forms, source documentation, case report forms, and investigational material accountability forms.
Completes data entry and query resolution according to timelines with accuracy.