Study Coordinator I

Cayuse Holdings•Honolulu, HI

1d•Onsite

About The Position

The Study Coordinator I will provide services to government led clinical and translational studies. This role involves working directly with the Principal Investigator/designated POC to collect, organize, maintain, and disseminate patient data files. Key duties include reviewing patient records for study eligibility, screening, enrolling, and monitoring study subjects, obtaining specimens for laboratory analysis, performing statistical data analysis, and providing written reports of findings. The position aligns with Cayuse’s core values of Innovation, Excellence, Collaboration, Adaptability, and Integrity by fostering technical solutions that meet customer needs, promoting teamwork, and prioritizing quality in deliverables.

Requirements

Minimum Bachelor of Science in Biomedical science field or nursing. Biomedical degree with clinical or translational experience.
Minimum 2 years clinical trial or laboratory study experience.
Familiarity with statistical analysis and preparing manuscripts for publication
Must be able to pass a background check. May require additional background checks as required by projects and/or clients at any time during employment.
Ability to communicate well with others, both orally and in writing, using technical and nontechnical language
Ability to perform a wide variety of duties and responsibilities.
Ability and willingness to quickly learn and put to use new skills and knowledge brought about by rapidly changing information and/or technology.
Close attention to detail required with ability to process and apply diverse and complex amounts of data.
Must possess problem-solving skills.
Ability to respond effectively to customers with a sense of urgency.
Proficient in Microsoft and Adobe toolsets, including Excel, Word, PowerPoint, Acrobat, etc.
Ability to forge new relationships, individual and teaming in nature.
Must be a Self-starter, that can work independently and as part of a team.

Responsibilities

Ability to conduct clinical and translational studies including the following: chart reviews, specimen processing, data management, interacting with physicians, scientists, nurses and other laboratory personnel.
Must be able to prepare oral and written presentations (as reflected in resume by publications, posters or podium presentations at national conferences, delivery of lectures or scientific presentations, thesis) based on data analysis and study summary.
Demonstrated ability (i.e. former work history of managing multiple research studies or clinical trials) to manage multiple clinical and translational studies simultaneously and develop policies and procedures for clinical study execution and oversight.
Other duties as assigned.