Experienced Clinical Research Associate, Multi-Sponsor, France

Conduct clinical monitoring visits, administer protocol and related study training, and ensure the quality and integrity of study site practices in accordance with good clinical practice and applicable regulations.

Requirements

• Bachelor's Degree in scientific discipline or health care
• Prior 2 years clinical oncology experience
• Computer skills including proficiency in Microsoft Word, Excel, and PowerPoint
• Written and verbal communication skills
• Organizational and problem-solving skills
• Effective time and financial management skills

Benefits

• Generous Paid Time Off
• 401k Matching
• Retirement Plan