Clinical Research Coordinator, On-Site, Kansas City, Missouri

IQVIA•Kansas City, MO

1d•$36,600 - $106,800•Onsite

About The Position

Please note that this position is fully on-site at the site in Kansas City, MO Join a collaborative, patient-centered team where your contributions directly support groundbreaking studies and improved patient outcomes. This is more than just a CRC role — it’s a unique opportunity to deepen your expertise in clinical trial coordination, grow within a supportive environment that values professional development, and make real progress toward your career goals. It’s an ideal fit for a hardworking, driven, and passionate individual who thrives in a fast-paced, team-oriented setting and is eager to make a meaningful impact through clinical research. Overview: This individual will play a key role in assisting in the conduct of clinical trial activities, in accordance with all applicable regulations governing the conduct of clinical trials. The primary skills include logical thinking, ability to prioritize, “can-do” attitude, the ability to adapt quickly to changing business conditions, strong interpersonal and team building skills. The employee, working closely with study team members, will achieve study objectives and corporate goals.

Requirements

Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines
Clinical Research Coordinator experience within a similar setting
Clinical skills experience including obtaining vitals, phlebotomy, EKG, etc.
Knowledge and experience of site operations and the drug development process
Effective communication
Computer proficiency in use of Microsoft Word, Excel

Responsibilities

Ability to coordinate as primary CRC 1-3 studies on average of low to medium complexity, with oversight by a manager or higher-level CRC. May assist as back-up CRC on other studies
Develops and implements patient recruitment strategies; actively recruits to ensure enrollment targets are achieved
Obtains informed consent of research subjects
Develops strong working relationships and maintain effective communication with study team members
Completes all protocol related training
Performs patient/research participant scheduling
Collects patient/research participant history
Collects and maintains source documentation
Manages inventory and administers test articles/investigational product to participants
Performs data entry and query resolution
Supports the collection and review of required essential study documents and reports. Order supportive study supplies (e.g., contracts, IXRS, lab kits, nonclinical supply materials, imaging, and laboratory handling manuals, etc.)
Adheres to an IRB approved protocol
Supports the safety of research subjects, report adverse events
Coordinates protocol related research procedures, study visits, and follow-up
Facilitates pre-study, site qualification, study initiation, monitoring visits, and study close out activities
Collects, processes and ships laboratory specimens
May be asked to perform special project responsibilities and travel to other clinic locations, within the area, when needs arise
Complies with Avacare and Sponsor policies, standard operating procedures (SOPs) and guidelines
Performs other duties as assigned