Bilingual Clinical Research Coordinator I – OB/GYN Trials

Yale University; New Haven (CT); On-site; USD 62,000 - 92,000; Full time

Job summary

Yale University in New Haven is seeking a Clinical Research Coordinator I in the Department of OBGYN and Division of Maternal-Fetal Medicine to support clinical trials. The CRC I will oversee, plan, and track activities, ensuring protocol adherence and patient safety.

Strong communication and bilingual English/Spanish skills are essential as you interact with diverse teams. Responsibilities include patient recruitment, consent, enrollment, and coordination across multidisciplinary teams, with

Qualifications

• Experience with patient recruitment and consent.
• Fluent in English and Spanish; willing to learn phlebotomy.
• Knowledge of GCP, FDA regulations, and HIPAA.
• Ability to manage multiple studies with minimal supervision.
• Strong communication and professionalism.

Responsibilities

• Oversee and coordinate all trial activities for low to moderately complex studies.
• Screen patients, determine eligibility, obtain informed consent, enroll participants.
• Maintain documentation and ensure regulatory compliance with ICH/GCP.
• Coordinate with investigators and study teams; monitor adverse events.

Skills

Patient recruitment

Informed consent

English/Spanish

Regulatory knowledge

Independent work

Education

Bachelor's degree in health-related discipline

Tools

EMR

Clinical trial management systems

Job description

Yale University in New Haven is seeking a Clinical Research Coordinator I in the Department of OBGYN and Division of Maternal-Fetal Medicine to support clinical trials. The CRC I will oversee, plan, and track activities, ensuring protocol adherence and patient safety.

Strong communication and bilingual English/Spanish skills are essential as you interact with diverse teams. Responsibilities include patient recruitment, consent, enrollment, and coordination across multidisciplinary teams, with