Site Activation Partner
Parexel
full-time
Posted on:
Location Type: Remote
Location: Brazil
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Tech Stack
About the role
- Lead or support operational activities from start up to close out for assigned studies
- Coordinate activities and document management during start up towards high quality Investigator Initiation Package
- Prepare and submit regulatory documents for internal approval
- Manage timely communication and documentation between client and central ethics committees
- Ensure maintenance of IRB/Ethics activities and timely filing of documents
Requirements
- Minimum 2 years relevant experience in clinical site management
- Knowledge of clinical trial methodologies
- Understanding of ICH/GCP and FDA regulations
- Must be fluent in local language and in English
- Good technical skills and ability to learn multiple systems
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
clinical site managementregulatory document preparationdocumentation managementinvestigator initiation package preparationcommunication management
Soft Skills
organizational skillscommunication skillsteam collaboration