Clinical Research Associate

Job Description

" A multi-tasked individual with a minimum 2 years of experience in a clinical research coordinator role.

" College degree in medicine, science, health, or equivalent.

" Performs management of research activities to ensure the collection of accurate clinical data within given timeline.

" Knowledge of ICG GCP guidelines and expertise to review, evaluate medical data and all applicable local laws and regulations.

" Demonstrated knowledge of all components of the research process as it pertains to clinical trials and studies, i.e., IRB procedures and processes, data management, etc

" Experience in selection and management of vendors/CROs (Central Lab, IVRS, EDC)

" Track progress of clinical studies with regard to budget, study milestones, and deadlines.

" Recruiting & enrolment of patients who meet eligibility criteria, scheduling, completing CRFs.

" Able to solve complex problems, prioritize multiple tasks, plan proactively and accomplish goals within project in a dynamic team environment

" Participate in study audits, as applicable

Experience

" Study Coordinator, Clinical Manager, Clinical Research Associate, Clinical Research Associate, Clinical Research Regulatory

Skills

" Attention to detail, analytical, organized, interpersonal communication, multitasking.