North AmericaFull TimeHealthcare
Remotely
crmgcpclinical researchsite monitoringrisk based monitoringsite engagementich gcpregulatory knowledge
Also available on
Job Description
📋 Description
- Primary contact for investigative site; connect stakeholders and sites.
- Train and motivate site staff and PI on trial goals and patient treatment.
- Conduct site evaluation, training, monitoring per protocol and regulations.
- Develop site engagement strategies; report progress using CRM tools.
- Link protocol, science, and trial execution for recruitment and retention.
- Mentor less experienced CRAs; participate in global/local initiatives.
🎯 Requirements
- Tertiary qualification in health-related field preferred.
- At least 1 year clinically-related experience; 6 months in trial monitoring.
- Knowledge of regulatory requirements, ICH/GCP guidelines.
- Strong collaboration, planning, organizational skills.
- Proficiency with technology/tools for patient-centric site support.
- Excellent communication; ability to build site partnerships.
🎁 Benefits
- Comprehensive benefits package; PTO, medical/dental/vision insurance, 401(k).
- Eligibility to participate in incentive programs.
- Equal opportunity employer; diverse, inclusive environment.