Cancer Clinical Research Coordinator 2 - EDD
@ Stanford University

Stanford, CA
$86,248
On Site
Full Time
Posted 1 day ago

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Job Details

Cancer Clinical Research Coordinator 2 - EDD

The Stanford Cancer Institute (SCI) is a National Cancer Institute-Designated Comprehensive Cancer Center known for its dynamic, growing environment. The position involves coordinating clinical trials in early drug development and managing key research studies at one of the top cancer centers in the country.

Key Responsibilities

  • Oversee subject recruitment and study enrollment.
  • Manage data collection, reporting, and analysis.
  • Develop project schedules and lead team meetings.
  • Mentor staff and ensure regulatory compliance.
  • Collaborate with investigators and sponsors, and monitor safety events.

Qualifications

Bachelor's degree in a related field with two years of clinical research experience or equivalent combination is required. Proficiency in Microsoft Office, database applications, and familiarity with HIPAA, FDA, and IRB regulations is essential.

Additional Information

This role offers a hybrid work arrangement. The position works within the Cancer Clinical Trials Office and contributes to early drug development research. Compensation ranges from $86,248 to $100,158 per annum. Stanford University offers a comprehensive benefits package and is committed to equal employment opportunity and reasonable accommodations.

Key skills/competency

  • Cancer Research
  • Clinical Trials
  • Data Management
  • Regulatory Compliance
  • Early Drug Development
  • Subject Recruitment
  • Project Coordination
  • Mentorship
  • Safety Monitoring
  • Stakeholder Collaboration

How to Get Hired at Stanford University

🎯 Tips for Getting Hired

  • Customize your resume: Highlight clinical research and data management experience.
  • Research Stanford University: Understand their cancer research mission.
  • Emphasize regulatory skills: Mention HIPAA, FDA, and IRB experience.
  • Prepare for interviews: Review early drug development case studies.

📝 Interview Preparation Advice

Technical Preparation

Review clinical trial protocols thoroughly.
Study data collection and analysis methods.
Brush up on FDA and IRB guidelines.
Practice project scheduling and system management.

Behavioral Questions

Describe a challenge in clinical research coordination.
Explain your teamwork experience under pressure.
How do you handle regulatory compliance issues?
Share a past experience mentoring junior staff.

Frequently Asked Questions