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Research Associate for Clinical Studies
2 months ago
We are a forward-thinking biotech firm focused on pioneering research and clinical advancements in oncology. Our recent achievements in securing FDA approvals highlight our dedication to progress and excellence in cancer therapies.
Why Work With Us?
- Attractive Salary Structure
- Substantial Equity Options
- Flexible Work Schedules
- Career Development Opportunities
As a Clinical Research Associate (CRA) at Jobot, you will collaborate closely with our Clinical Operations Director to manage site monitoring tasks for our clinical trials. Your role will encompass conducting site assessments, training personnel, ensuring data integrity, and upholding regulatory compliance.
Key Duties
- Conduct site monitoring visits according to established plans and standard operating procedures
- Educate investigators and team members on study protocols
- Guarantee data accuracy and prompt resolution of inquiries
- Document protocol deviations and compliance issues
- Monitor and report on the progress of assigned sites
- Facilitate Investigator Meetings and training sessions
- Oversee inventory and distribution of clinical materials
- Engage in Clinical Trial Team Meetings
- Execute additional responsibilities as required
To excel in this position, candidates should possess:
- A Bachelor’s Degree in life sciences or nursing
- A minimum of 5 years of experience in clinical research
- Preferred experience in oncology
- Familiarity with GCP Regulations and ICH Guidelines
- Proficiency in Microsoft Office Suite
- Strong communication abilities
- Willingness to travel up to 70% of the time