Clinical Research Associate II - Oncology MN

📋 Description

• Considered as the primary point of contact for the investigative site. High level of competency or
• Aligns, trains and motivates the site staff and principal investigator on the goals of the clinical
• Conducts site evaluation, site training, routine, and site closure monitoring activities with
• Advanced understanding of site engagement and ability to customize site engagement strategy for
• Advanced level of competency connecting the study protocol, scientific principles and clinical
• Possesses experienced level of competency to mentor and train less experienced CRAs on various

🎯 Requirements

• Appropriate tertiary qualification in health related disciplines (Medical, Scientific, Nursing)
• Minimum of 1 year of clinically related experience, of which a period of 6 months is required in
• Familiar with risk-based monitoring approach, on-site and off-site activities.
• Knowledge of appropriate therapeutic area indications is preferred with ability to apply scientific
• Advanced knowledge on existing and emerging local regulatory and legal requirements, ICH/GCP
• Strong cross-functional collaboration skills, planning, and organizational skills; ability to work

🎁 Benefits

• Comprehensive benefits package including paid time off, medical, dental, vision insurance, and
• Eligible for short-term incentive programs
• Competitive compensation range based on job grade and geographic location