Role Overview:
- Oversee site management, monitoring oversight, and clinical trial operations.
- Ensure compliance with GCP, regulatory requirements, and company SOPs.
- Work closely with cross-functional teams and clinical sites to drive study execution.
Basic Qualifications:
- Bachelor’s degree in life sciences, nursing, or a related field.
- 2+ years of experience in on-site clinical monitoring and 2+ years of CTM experience.
- Strong knowledge of ICH-GCP, FDA, EMA, and applicable clinical trial regulations.
What do we offer?
- Competitive rates for Health, Dental, and Vision Insurance.
- Generous vacation time and paid holidays.
- 401(k) with company match.
Immatics
Immatics is dedicated to making a significant difference in the lives of cancer patients. They are a global frontrunner in precision targeting of PRAME, found in over 50 cancers, with cutting-edge science and a strong clinical pipeline.