Clinical Research Coordinator
KS - Kansas City On-site
$56,160–$76,960 a yearJobFig found this opening at its original source and checks that it remains available.
About the role
As an on-site Clinical Research Coordinator (CRC), you will provide technical and administrative support to your assigned clinical operations team in the field as well as direct patient care of research study participants. You work with a high attention to detail, reviewing documentation, coordinating clinical study project details, and maintaining data systems - all with a sense of urgency aligned with that of our customers. The position will involve the conduct of trial coordinator activities for EmVenio Research’ decentralized network. In this role the CRC is accountable for the regulatory compliance and performance of assigned mobile clinics and clinician teams conducting decentralized trials as well as patient engagement, and screening.
What you'll bring
- Bachelor's degree (B.
- A. / B.
- S.) from four-year college or university or equivalent combination of education, training, and experience that provides the individual with the required knowledge, skills, and abilities
- Excellent computer skills, proficient in MS Word, Excel, PowerPoint and ability to obtain knowledge and master all clinical trial database systems.
- Proven ability to successfully coordinate multiple studies adhering to regulatory and institutional guidelines.
- Proven ability to communicate effectively within an interdisciplinary team to ensure safe, efficient, quality patient care, both in-person and virtually.
- Excellent organizational skills and strong attention to detail, with proven ability to handle multiple tasks efficiently and effectively.
- Ability to effectively analyze project specific data/systems to ensure accuracy and efficiency.
- Flexibility to reprioritize workload to meet changing project timelines.
- Responsible for adhering to FDA Good Clinical Practices, FDA regulations, EmVenio Research /Client Standard Operating Procedures and Working Practice Documents regulations for all non-clinical/clinical aspects of project implementation, execution, and closeout.
- Ability to successfully complete EmVenio Research clinical training program.
- Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.