immatics
Senior Clinical Research Associate
At a Glance
- Location
- Work (USA), United States
- Employment
- Full time
- Experience
- 4+ years
- Compensation
- impact on patients globally. $120,000 to $135,000 At Immatics, we believe in i
- Posted
- 2026-05-28
Key Requirements
Required Skills
Domain Knowledge
- Biotech
- Clinical
- Pharmaceutical
Benefits & Perks
sion Insurance 4 weeks of vacation, granted up front each year a
Health, Dental, and Vision Insurance 4 weeks of vacation, granted up front e
Requirements
4+ years of on-site monitoring experience within the pharmaceutical or biotechnology industry, including all clinical monitoring visit types
Strong knowledge of ICH-GCP, FDA, EMA, and applicable clinical trial regulations
Demonstrated experience managing clinical trial sites, monitoring activities, and clinical trial documentation
Proficiency with clinical trial systems and tools (e.g., CTMS, eTMF, Microsoft Office)
Experience in oncology clinical trials or related therapeutic areas
Experience mentoring or training junior CRAs and supporting cross-functional clinical operations activities
Compensation & Benefits
Innovative Environment:
Help to pioneer advancements in cancer immunotherapy.
Collaborative Culture:
Be part of
a diverse team dedicated to your professional growth.
Global Impact:
Responsibilities
We are seeking a Senior Clinical Research Associate (CRA) to support our Clinical Operations team.
The Senior CRA will be responsible for overseeing clinical trial site management and monitoring activities to ensure compliance with ICH-GCP, regulatory requirements, and company SOPs.
In this role, you will partner closely with clinical sites and cross-functional teams to support high-quality study execution, patient recruitment, and operational excellence across clinical trials.