CLINICAL RESEARCH COORDINATOR

Clinical Trials Investment Group; Town of Florida (NY); On-site; USD 60,000 - 80,000; Full time

Job summary

Clinical Trials Investment Group is seeking a full-time Clinical Research Coordinator fluent in English and Spanish to support investigators in preparing and executing trials. The role requires coordinating visits, managing study data, handling labs, and ensuring subject safety.

Strong organization, communication, and time management skills are essential, along with ICH and GCP certification. The position emphasizes screening and enrolling participants, maintaining logs, and providing hands-on

Qualifications

• Must be bilingual (English/Spanish).
• 2+ years of experience required.
• Strong computer skills and knowledge of medical terminology.
• Knowledge of Office 365.
• Excellent organization and communication skills.
• Excellent time management.
• ICH and GCP certified.

Responsibilities

• Coordinate and support investigators to prepare for and execute studies.
• Recruit and screen subjects for clinical trials and maintain logs.
• Orient subjects to the study and maintain source documentation as per protocol.
• Schedule and conduct study visits and procedures; collect and record data.
• Handle lab testing, specimen collection and lab logistics.
• Monitor subject safety and report adverse events to medical personnel.
• Troubleshoot study-related questions and attend sponsor trainings.

Skills

Bilingual English/Spanish

Organization

Communication

Time management

Medical terminology

Tools

Office 365

Job description

Job 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 Description

WE 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.