Senior Clinical Trial Associate — Startup & TMF Expert

ALX Oncology; South San Francisco (CA); On-site; USD 60,000 - 80,000; Full time

Benefits offered by this job

Flexible working models

Competitive benefits

Opportunity for personal and professional growth

Job summary

ALX Oncology in South San Francisco is seeking a Clinical Trial Associate to support various clinical trial activities. The role includes managing Trial Master Files, assisting with site activation, and ensuring compliance with regulatory standards.

The ideal candidate has 1-3 years of relevant experience, proficiency in MS Office and eTMF systems, and strong organizational skills. Join an environment offering professional growth and competitive benefits.

Qualifications

• 1-3 years of experience in clinical research (CRO or sponsor environment).
• Experience supporting multiple clinical trials, preferably in oncology.
• Working knowledge of ICH-GCP regulations.

Responsibilities

• Support clinical operations by managing key study execution activities.
• Maintain electronic Trial Master Files (eTMF) and ensure regulatory compliance.
• Act as a point of contact for clinical sites and vendors.

Skills

Understanding of the drug development process

Strong verbal and written communication

Problem-solving

Adaptability to shifting priorities

Strong organizational skills

Education

Four-year degree in a related field

Tools

MS Office Suite (Excel, Word, PowerPoint)

eTMF/EDC systems (e.g., Veeva Vault)

CTMS

Job description

ALX Oncology in South San Francisco is seeking a Clinical Trial Associate to support various clinical trial activities. The role includes managing Trial Master Files, assisting with site activation, and ensuring compliance with regulatory standards.

The ideal candidate has 1-3 years of relevant experience, proficiency in MS Office and eTMF systems, and strong organizational skills. Join an environment offering professional growth and competitive benefits.