Clinical Research Coordinator - Study Enrollments & Data

Dm Clinical Research Group; Philadelphia (Philadelphia County); On-site; USD 55,000 - 75,000; Full time

Job summary

Dm Clinical Research Group is seeking a Clinical Research Coordinator I to work at the site to ensure quality research aligns with sponsor protocol, FDA regulations, and ICH/GCP guidelines, delivering high-quality data.

The role involves training, patient recruitment, consent discussions, data entry, ALCOA-C documentation, and coordinating with laboratories and sponsor teams to meet enrollment and study timelines.

Qualifications

• 1+ years of CRC experience, preferably coordinating vaccines in a private setting.
• 2+ years of experience as a research assistant or related clinical research role.
• ACRP certification preferred.
• Registered Medical Assistant certification preferred.

Responsibilities

• Complete DMCR-required training, including ICH-GCP and IATA certifications.
• Conduct subject visits and protocol-required procedures; document timely.
• Data entry and query resolution per guidelines and sponsor expectations.
• Recruit and retain subjects; engage with participants and address concerns.
• Obtain informed consent and explain procedures, risks, benefits, and alternatives.
• Facilitate communication between patients, healthcare providers, and research staff.
• Submit administrative paperwork per timelines; liaise with teams and sponsor/CRO representatives.

Skills

Communication skills

English proficiency

Bilingual English/Spanish

Attention to detail

Data entry

Education

High School Diploma

Bachelor's degree preferred

Job description

Dm Clinical Research Group is seeking a Clinical Research Coordinator I to work at the site to ensure quality research aligns with sponsor protocol, FDA regulations, and ICH/GCP guidelines, delivering high-quality data.

The role involves training, patient recruitment, consent discussions, data entry, ALCOA-C documentation, and coordinating with laboratories and sponsor teams to meet enrollment and study timelines.