Clinical Trials Coordinator (Medical Assistant)

SmartRecruiters, Inc.; New Haven (CT); On-site; USD 136,000 - 194,000; Full time

Job summary

Global Channel Management is seeking a Clinical Study Coordinator to support screening, visits, and data entry within a clinical team. You will handle day-to-day study activities and assist with coordinating study processes in a compliant environment.

The role requires 3–5 years of experience in study coordination, and involves front desk duties, appointment scheduling, medical records management, and data entry using the EMR system, with adherence to regulatory guidelines.

Qualifications

• Associate or Bachelor’s degree required.
• 3–5 years of relevant experience in study coordination or clinical research.
• Responsible for coordinating day-to-day execution of study activities and related financial responsibilities while adhering to ICH GCP, scientific, medical and ethical principles.

Responsibilities

• Coordinate day-to-day study activities including screening, follow-up, repeat and final visits.
• Manage front desk activities: greet patients, schedule appointments, medical record management, and data entry.
• Enter medical data into the electronic medical records database and maintain familiarity with medical terminology.

Skills

Study coordination

Education

Associate or Bachelor’s degree

Tools

EMR database

Job description

Global Channel Management is seeking a Clinical Study Coordinator to support screening, visits, and data entry within a clinical team. You will handle day-to-day study activities and assist with coordinating study processes in a compliant environment.

The role requires 3–5 years of experience in study coordination, and involves front desk duties, appointment scheduling, medical records management, and data entry using the EMR system, with adherence to regulatory guidelines.