Clinical Research Coordinator I — Growth in Clinical Trials

Dm Clinical Research Group; Florida; On-site; USD 42,000 - 56,000; Full time

Job summary

Dm Clinical Research Group in Doral, FL is seeking a Clinical Research Coordinator I to support at-site coordination of clinical trials, ensuring adherence to sponsor protocols, FDA regulations, and ICH/GCP guidelines. The CRC I will assist with patient visits, informed consent discussions, data entry and timely documentation to deliver quality data for sponsors.

The role requires strong English communication, attention to detail, and the ability to multi-task across study activities.

Qualifications

• High School Diploma or equivalent required.
• Bachelor's degree a plus.
• ACRP certification preferred.
• Registered Medical Assistant certification or equivalent preferred.

Responsibilities

• Conduct patient visits and study procedures per protocol.
• Ensure adherence to ALCOA-C standards for documentation.
• Complete data entry and resolve queries per sponsor expectations.
• Coordinate with Laboratory, Data, Administrative staff and investigators.
• Assist with subject recruitment and retention efforts.
• Obtain informed consent and explain risks/benefits to participants.
• Communicate effectively with patients, providers and staff.
• Submit administrative paperwork within timelines.

Skills

Detail oriented

Multi-tasking

Communication skills

English proficiency

Bi-lingual English/Spanish

Education

High School Diploma or equivalent

Bachelor's degree preferred

Foreign Medical Graduates preferred

Job description

Dm Clinical Research Group in Doral, FL is seeking a Clinical Research Coordinator I to support at-site coordination of clinical trials, ensuring adherence to sponsor protocols, FDA regulations, and ICH/GCP guidelines. The CRC I will assist with patient visits, informed consent discussions, data entry and timely documentation to deliver quality data for sponsors.

The role requires strong English communication, attention to detail, and the ability to multi-task across study activities.