Clinical Research Coordinator I: Study Logistics & Data

Dm Clinical Research Group; Florida; On-site; USD 42,000 - 62,000; Full time

Job summary

Dm Clinical Research Group is seeking a Clinical Research Coordinator I to ensure quality research at assigned investigative sites, in accordance with sponsor protocol, FDA regulations, and ICH/GCP guidelines.

You will assist with study enrollment, data integrity, and training to maintain timelines and sponsor expectations. The role requires collaboration with researchers, participants, and sponsor teams to deliver reliable data.

Qualifications

• High School Diploma or equivalent required.
• Bachelor's degree preferred.
• ACRP or equivalent certification preferred.
• Proficient English; bilingual English/Spanish preferred.

Responsibilities

• Conduct subject visits and protocol-required procedures and document them promptly.
• Data entry and query resolution per sponsor and internal guidelines.
• Participate in subject recruitment and retention efforts.
• Conduct patient consent discussions and ensure comprehension of procedures, risks, and benefits.
• Coordinate with Laboratory, Data, Administrative staff, Investigators, participants, and Sponsor/CRO teams.

Skills

IATA Certification

ICH-GCP

ALCOA-C

Data entry

Recruitment

Consent discussions

Bilingual English/Spanish

Communication

Clinical Research

Education

High School Diploma

Bachelor's degree preferred

Job description

Dm Clinical Research Group is seeking a Clinical Research Coordinator I to ensure quality research at assigned investigative sites, in accordance with sponsor protocol, FDA regulations, and ICH/GCP guidelines.

You will assist with study enrollment, data integrity, and training to maintain timelines and sponsor expectations. The role requires collaboration with researchers, participants, and sponsor teams to deliver reliable data.