Travel Clinical Research Coordinator

CARE

. Utilize Good Clinical Practices (GCP) in the process of screening, as well as enrolling and closely monitoring clinical research study subjects while ensuring protocol and regulatory compliance.

Posted 4/22/2026full-timeRemote • 🇺🇸 United StatesMid-LevelSenior💰 $70,000 - $100,000 per yearWebsite

Tech Stack

Tools & technologies

Google Cloud PlatformOracle

About the role

Key responsibilities & impact

Utilize Good Clinical Practices (GCP) in the process of screening, as well as enrolling and closely monitoring clinical research study subjects while ensuring protocol and regulatory compliance.
Assume a greater study workload and overall study responsibility.
Maintain strong and clear communication with clinical research teams and participants.
Help with study preparation by reviewing protocols and assisting in the creation of recruitment materials.
Manage studies by integrating new trials, maintaining organized files, and ensuring compliance with FDA regulations.
Prescreen study candidates, obtain informed consent, and monitor patient progress.
Record data legibly, maintain accurate logs, and assist with regulatory filings.

Requirements

What you’ll need

Bilingual proficiency required: Must be fluent in both English and Spanish, with the ability to effectively communicate (written and verbal) in both languages.
Excellent working knowledge of clinical trials, medicine and research terminology
Excellent working knowledge of federal regulations, good clinical practices (GCP), good documentation practices (GDP), and ALCOA-C+
Ability to communicate and work effectively with a diverse team of professionals
Strong organizational, prioritization and leadership skills and capabilities with a strong attention to detail
Strong computer skills with demonstrated abilities using clinical trials database, IVR systems, electronic data capture, MS word, and excel.
Proficiency with technology used to support the clinical trial industry. CTMS systems like CRIO, clinical conductor, Clinical Ink; EDC systems like MediData, Oracle, and Inform; ePRO, eConsent and IWRS/IXRS, etc.
Critical thinker and problem solver
Friendly, outgoing personality; maintain a positive attitude under pressure
High level of self-motivation and energy
Excellent professional writing and communication skills
Ability to work independently in a fast-paced environment with minimal supervision.
BS in nursing, pharmacy or other related science or combination of equivalent education preferred in the Arts or Sciences preferred
RN or LPN preferred
Research Professional Certification- CRCC or exam eligibility preferred
A minimum of 3 to 4 years Clinical Research experience
A minimum of 2 years prior Clinical Research Coordinator experience, management level preferred.

Benefits

Comp & perks

Paid Time Off (PTO) and Company Paid Holidays
100% Employer paid medical, dental, and vision insurance plan options
Health Savings Account and Flexible Spending Accounts
Bi-weekly HSA employer contribution
Company paid Short-Term Disability and Long-Term Disability
401(k) Retirement Plan, with Company Match

ATS Keywords

✓ Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools

clinical trialsGood Clinical Practices (GCP)Good Documentation Practices (GDP)ALCOA-C+data recordingregulatory complianceinformed consentclinical research terminologyproblem solvingorganizational skills

Soft Skills

bilingual proficiencycommunication skillsleadership skillsattention to detailself-motivationpositive attitudeability to work independentlyteam collaborationprioritization skillscritical thinking

Certifications

Research Professional CertificationCRCCRNLPN