Clinical Research Coordinator II — Drive Multi-Site Studies

Alcanza Clinical Research; Fredericksburg (VA); On-site; USD 55,000 - 75,000; Full time

Benefits offered by this job

Medical, dental, vision insurance

401(k) with safe harbor match

Life insurance

Paid time off

Job summary

Alcanza Clinical Research is seeking a Clinical Research Coordinator II for our Fredericksburg site. The role involves coordinating studies in compliance with FDA, GCP, and ICH guidelines, including patient screening, consent, visits, and data entry.

The candidate should have a Medical Assistant diploma or equivalent and 2+ years of clinical research coordination experience; bilingual English/Spanish is a plus, with credentialing such as CCRC/CCRP preferred.

Qualifications

• A Medical Assistant diploma, LPN/LVN, EMT credential AND 2+ years of clinical research coordination experience is required.
• CCRC or CCRP credential and BLS certification are preferred.
• Bi-lingual English/Spanish proficiency is a plus.

Responsibilities

• Screening patients for study enrollment.
• Obtaining patient consents and conducting follow-up visits.
• Documenting in source charts and data entry in EDC.
• Obtaining vital signs and ECGs; basic lab procedures per protocol.
• Managing study-specific supplies and scheduling visits.
• Maintaining logs, patient confidentiality, and HIPAA compliance.
• Participating in site initiation visits and investigator meetings.

Skills

Clinical procedures

Computer proficiency

Organizational skills

Communication

Independence / initiative

HIPAA/compliance

Education

Medical Assistant diploma

LPN/LVN

EMT credential

CCRC/CCRP credential

BLS certification

Tools

EHR systems

Microsoft Office

Job description

Alcanza Clinical Research is seeking a Clinical Research Coordinator II for our Fredericksburg site. The role involves coordinating studies in compliance with FDA, GCP, and ICH guidelines, including patient screening, consent, visits, and data entry.

The candidate should have a Medical Assistant diploma or equivalent and 2+ years of clinical research coordination experience; bilingual English/Spanish is a plus, with credentialing such as CCRC/CCRP preferred.