Senior Clinical Research Associate – Brazil
Precision For Medicine
full-time
Posted on:
Location Type: Remote
Location: Brazil
Visit company websiteExplore more
Job Level
About the role
- Independently oversees all aspects of study site management to ensure patient safety is protected
- Provides guidance at the site and project level towards audit readiness standards and supports preparation for audit
- Establishes, updates, tracks and maintains study specific trial management tools/systems
- Manages site start up procedures including the feasibility and recruitment of potential investigators
- Documents activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents
- Prepares for and attends Investigator Meetings and/or sponsor face-to-face meetings
Requirements
- 4-year college degree or equivalent experience in a scientific or healthcare discipline
- 5 years or more as a CRA in either a CRO or pharmaceutical/biotech industry or equivalent, relevant experience and/or demonstrated competencies
- Significant site management experience or equivalent experience in clinical research
- Ability to communicate both verbally and in writing at the English proficiently (Professional level)
Benefits
- Health insurance
- Retirement plans
- Paid time off
- Flexible work arrangements
- Professional development
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
study site managementaudit readinesstrial management toolssite start up proceduresfeasibility assessmentinvestigator recruitmentdocumentation managementproject documentationinvestigator meetingssponsor meetings
Soft Skills
communicationguidanceorganizational skillsindependenceattention to detail
Certifications
4-year college degreeCRA certification