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Clinical Research Associate (CRA) Monitor – Consultant
Ividata Life Sciences. Manage the selection, start-up, monitoring, and close-out of investigator sites .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in managing clinical trial processes, including site selection, monitoring, and patient safety reporting. Proficient in collaborating with cross-functional teams and conducting interventional clinical trials, particularly in oncology.
Highest-signal resume keywords
Clinical Research Associate (CRA) MonitoringPhase II And III Clinical TrialsOncology ExperiencePatient Safety MonitoringProfessional Proficiency In English
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
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Hard Skills
Site SelectionMonitoring VisitsSource Data VerificationAdverse Event ReportingCase Report Form (CRF) Management
Soft Skills
CollaborationCommunication
Certifications & Qualifications
Master’s DegreePhDPharmacy DegreeFARCCRA
Industry Keywords
Clinical ResearchPharmaceuticalBiotechnologyInterventional TrialsSerious Adverse Events (SAEs)
About the role
Key responsibilities & impact- Manage the selection, start-up, monitoring, and close-out of investigator sites
- Conduct on-site and/or remote monitoring visits
- Ensure patient safety monitoring and reporting of serious adverse events (SAEs)
- Verify source data against the case report form (CRF/eCRF)
- Collaborate with project managers, medical teams, and investigators
- Contribute to projects for pharmaceutical and biotechnology clients
Requirements
What you’ll need- Education: Master’s degree or equivalent in a scientific discipline (Master’s degree, engineering degree, PhD, or Pharmacy degree), or specialized training in clinical research (FARC/CRA)
- At least 2–3 years of experience as a Clinical Research Associate (CRA) Monitor
- Proven experience in Phase II and III interventional clinical trials required
- Strong oncology experience highly preferred
- Professional proficiency in English, both written and spoken
- Availability for 7–8 business trips per month
Benefits
Comp & perks- Hybrid working arrangements with the possibility of remote work
- Stimulating and collaborative environment
- High-impact assignments at the heart of healthcare innovation
- Collaboration with passionate experts and leading organizations in the sector
- Opportunities to make a real impact through consultants’ ideas and expertise