Clinical Study Oversight Professional

2 weeks ago


San Diego, California, United States Jobot Full time
Exciting Career Opportunity with Competitive Benefits and Growth Potential

We are a leading biotech firm focused on pioneering research and clinical development in oncology. Our recent FDA approvals highlight our dedication to innovation and progress in cancer therapies.

Why consider a position with us?
  • Attractive Salary Structure
  • Comprehensive Equity Packages
  • Flexible Work Options
  • Career Development Opportunities
Position Summary

As a Clinical Research Associate (CRA) at Jobot, you will collaborate closely with our Clinical Operations Director to manage site monitoring activities for clinical trials. Your role will encompass conducting site assessments, training personnel, ensuring data integrity, and upholding compliance with regulatory standards.

Core Responsibilities
  • Conduct site monitoring visits in accordance with monitoring protocols and standard operating procedures
  • Educate investigators and staff 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 supplies
  • Engage in Clinical Trial Team Meetings
  • Execute additional tasks as required
Required Qualifications

To excel in this position, candidates should possess:
  • 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
If you are eager to make a significant impact in the field of oncology research, we invite you to explore this rewarding opportunity.

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