Description

Job DescriptionJob Description

Clinical Research Site seeking full time clinical research coordinator with experience. Must be Bilingual.

Responsibilities:

• Must be able to manage an coordinate accordingly
• Must provide clinical research support to investigators to prepare for and execute assigned research studies including, reviewing protocols, case report forms, study specific documents and electronic data capture systems use to record research data
• Recruit and screen subjects for clinical trials and maintain all logs
• Orient research subjects to the study
• Design and maintain source documentation based on protocol requirements
• Schedule and Execute study visits and perform all study procedures
• Collect, Record and maintain research subject study data according to protocol and SOPS
• Handle lab testing and analysis including preparation of specimen collection tubes and lab logistic
• Monitor subject safety and report adverse reaction to appropriate medical personnel
• Trouble shoot study related question and concerns and resolve all queries in a timely manner
• Attend all IM, SIV and other training session required by the sponsor

Requirements:

• Must be Bilingual ( English/Spanish)
• 2+ years of Experience
• Strong computer skills and knowledgable with medical terminology
• Knowledge of Office 365
• Excellent organization skills
• Excellent written and oral communication skills
• Excellent Time management
• ICH and GCP certified

Company DescriptionWE ARE A GROWING COMPANY WITH VARIOUS DOCTORS SERVING AS PI IN DIFFERENT AREAS OF PRACTICE. WE SPECIALIZE IN CLINICAL TRIALS WE DO NOT OFFER REGULAR MEDICAL SERVICES.Company DescriptionWE ARE A GROWING COMPANY WITH VARIOUS DOCTORS SERVING AS PI IN DIFFERENT AREAS OF PRACTICE. WE SPECIALIZE IN CLINICAL TRIALS WE DO NOT OFFER REGULAR MEDICAL SERVICES.