Travel CRC for Multi-Site Clinical Studies

Accel Research Sites; United States; On-site; USD 52,000 - 76,000; Full time

Benefits offered by this job

Medical, dental, vision insurance

401k with match

Life insurance

Job summary

Accel Research Sites is seeking a Travel Clinical Research Coordinator to support multi-site Phase I-IV studies under the Site Manager/Director. You will screen patients, obtain consents, coordinate visits, collect data, manage samples, and ensure compliance with FDA/GCP/ICH and HIPAA guidelines.

Responsibilities include site initiation, ongoing monitoring, adverse event reporting, regulatory submissions, and collaboration with investigators and sponsors to maintain study timelines and data

Qualifications

• Minimum Qualifications: Medical Assistant diploma, LPN/LVN, EMT credential AND 2+ years of clinical research coordination experience, or equivalent education/experience.
• Proficiency with basic clinical procedures (blood pressure, vitals, EKGs, phlebotomy) is highly preferred.

Responsibilities

• Screening of patients for study enrollment
• Patient consents
• Patient follow-up visits
• Documenting in source clinic charts
• Entering data in EDC and answering queries
• Obtaining vital signs and ECGs
• May perform basic lab procedures per protocol (blood collection, centrifuge, storage and shipping)
• Requesting and tracking medical record requests
• Updating and maintaining logs, chart filings
• Maintaining and ordering study specific supplies
• Scheduling subjects for study visits and reminders
• Building/updating source as needed
• Conducting monitoring visits and resolving issues
• Ensuring study reports and results are reviewed by investigator
• Filing SAE/Deviation reports and IRB as needed
• Documenting and reporting adverse events
• Reporting non-compliance
• Maintaining communication with clients and team
• ALCOAC documentation
• Complete start-up activities and training
• Prepare and attend site initiation visits and investigator meetings
• Assist with IRB functions and regulatory tasks
• Assist with training of new staff
• Assist with scheduling for visit capacity
• May set up/maintain technology for studies
• May assist with recruitment and enrollment
• May handle complex study assignments and community outreach
• Maintaining confidentiality of patients and information
• Performing all other duties as assigned

Skills

Computer literacy

Vital signs

EKG

Phlebotomy

Bilingual English/Spanish

HIPAA awareness

Attention to detail

Education

Medical Assistant diploma

LPN/LVN

EMT credential

Job description

Accel Research Sites is seeking a Travel Clinical Research Coordinator to support multi-site Phase I-IV studies under the Site Manager/Director. You will screen patients, obtain consents, coordinate visits, collect data, manage samples, and ensure compliance with FDA/GCP/ICH and HIPAA guidelines.

Responsibilities include site initiation, ongoing monitoring, adverse event reporting, regulatory submissions, and collaboration with investigators and sponsors to maintain study timelines and data