Sr. Clinical Trial Associate

Scorpion Therapeutics; Princeton (NJ); Hybrid; USD 85,000 - 125,000; Full time

Benefits offered by this job

Hybrid work arrangement

Job summary

Scorpion Therapeutics is seeking a Senior Clinical Trial Associate to support clinical operations for Phase 3 oncology studies (NSCLC and colorectal cancer) involving an investigational therapy. The role offers hybrid work arrangements and requires strong organizational and communication skills to manage administrative activities across study timelines.

The candidate will oversee eTMF and document management, vendor interactions, study budgeting, and regulatory compliance from start-up through

Qualifications

• Bachelor's degree in biological, health sciences or related field.
• 4+ years of experience in clinical study environments within CROs or pharma.
• Proficiency with CTMS and eTMF systems; knowledge of GCP, FDA regulations, and clinical trial processes from start-up to close-out.

Responsibilities

• Manage meeting logistics and study coordination activities.
• File documents and maintain study trackers and eTMF oversight.
• Coordinate vendor interactions and support study start-up and close-out processes.
• Assist with study budgeting, compliance, and cross-functional coordination.

Skills

Organizational skills

Communication

Problem-solving

Education

Bachelor's degree in biological/health sciences or related field

Tools

CTMS

eTMF

Job description

Role: Senior Clinical Trial Associate supporting clinical operations for Summit's oncology Phase 3 studies in NSCLC and colorectal cancer, with an investigational therapy (ivonescimab). Objectives include providing administrative support across study activities to ensure smooth trial execution.

Responsibilities encompass managing meeting logistics, document filing, study tracker maintenance, oversight of eTMF and vendor interactions, and supporting study start-up and close-out processes. They also assist with study budgeting, compliance, and cross-functional coordination.

Qualifications include a bachelor's in biological, health sciences, or related field; 4+ years of experience in clinical study environments within CROs or pharma; proficiency with CTMS and eTMF systems; and knowledge of GCP, FDA regulations, and clinical trial processes from start-up to close-out.

Preferred skills involve strong organizational, communication, and problem-solving abilities, with attention to detail and confidentiality.

High-value specifics include supporting Phase 3 oncology studies for NSCLC and colorectal cancer, with a focus on regulatory compliance, document management, and vendor oversight. The role is based in a hybrid setup, with no travel specified.