Clinical Research Associate

Responsibilities

• Oversee the development and execution of the clinical trial plans and protocols for Phase I-IV
• Maintain documentation and data evaluations
• Work collaboratively with the team to ensure monitoring activities meet study requirements
• Conduct on site field evaluations

Qualifications

• Experience with Oncology as a therapeutic indication
• 3+ years of clinical monitoring experience, specifically with Oncology
• Experience with the FDA or similar Regulatory and Accrediting administrations
• Bachelor’s degree in one of the life sciences or related background

Compensation

Salary Range: $120,000-$135,000
Comprehensive Benefits: Medical, Dental, Vision, 401k, and sick leave if required by law