FSP Clinical Research Associate II

Employer Industry

Clinical Research Organization (CRO)

• Salary up to $137,300
• Eligible for a discretionary annual bonus and robust benefits package including health insurance, retirement savings benefits, life insurance, and paid parental leave
• Supportive work environment that values employee contributions and ideas
• Opportunity for career advancement and professional growth within a midsized CRO
• Reasonable travel requirements, promoting a healthy work/life balance
• Fully remote position with flexibility for candidates located in the Midwest

• Oversee all aspects of study site management to ensure patient safety and data quality
• Conduct site visits, including pre-study, initiation, monitoring, and close‑out visits, in compliance with protocols and regulations
• Manage site start‑up procedures and assist with regulatory submissions and contract negotiations
• Communicate effectively with site personnel and project management to address protocol issues and implement necessary actions
• Perform data review activities and ensure compliance with trial management systems

• 4‑year college degree or equivalent experience in a scientific or healthcare discipline
• Minimum of two (2) years of experience as a CRA in a CRO or relevant clinical research experience
• Excellent communication and organizational skills
• Ability to travel overnight, with up to 60% travel on average based on regional requirements
• Fluency in English, and local language proficiency for non‑English speaking countries where applicable

• Graduate or postgraduate degree in a relevant field
• Experience monitoring oncology trials, especially in early phases
• Knowledge of monitoring EDC trials and EHR records
• Experience in biopharma or relevant therapeutic areas
• Relevant site start‑up experience, including feasibility and contract negotiations

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