Clinical Trial Associate

Scorpion Therapeutics; Boston (MA); On-site; USD 65,000 - 90,000; Full time

Job summary

Scorpion Therapeutics in Boston is seeking a Clinical Trial Associate to support oncology trials across all phases. You will coordinate start-up, monitoring, and close-out activities while ensuring GCP compliance and TMF integrity.

Work with CROs and vendors to track metrics, support inspection readiness, and maintain regulatory documentation. A bachelor’s degree in a scientific field and 1–2 years of clinical research experience are preferred.

Qualifications

• Bachelor’s degree in a scientific field.
• 1–2 years of clinical research experience or equivalent.
• Familiarity with GCP and FDA regulations.
• Experience with eTMF systems such as Veeva Vault.

Responsibilities

• Coordinate trial start-up, monitoring, close-out activities.
• Manage vendor and site documentation.
• Oversee TMF compliance using eTMF systems.
• Track study metrics and support inspection readiness.
• Collaborate with internal teams, CROs, and vendors.
• Assist with study documentation, site monitoring, and regulatory compliance.

Skills

Organizational skills

Communication skills

Documentation skills

Education

Bachelor's in a scientific field

Tools

Veeva Vault

Job description

Role

Clinical Trial Associate supporting operational execution of oncology clinical trials across all phases, ensuring compliance, milestone achievement, and efficient study conduct.

Responsibilities

• Coordinate trial start-up, monitoring, close-out activities
• Manage vendor and site documentation
• Oversee TMF compliance using eTMF systems
• Track study metrics and support inspection readiness
• Collaborate with internal teams, CROs, and vendors
• Assist with study documentation, site monitoring, and regulatory compliance

Qualifications

• Bachelor’s in a scientific field
• 1-2 years of clinical research experience or equivalent
• Strong organizational, communication, and documentation skills
• Familiarity with GCP, FDA regulations, and eTMF systems (e.g., Veeva Vault)

Preferred

• Experience in oncology
• CRO oversight
• Working in high-volume environments

HighValue

• oncology trials
• clinical operations
• GCP compliance
• CRO/vendor oversight
• eTMF management
• minimal travel

WorkSetup

primarily office-based with potential for some travel.