Job Description

Join Immatics and shape the future of cancer immunotherapy; one patient at a time! Immatics is at the forefront of immunotherapy innovation, working to harness the power of T cells to transform cancer treatment. Immatics is an exceptional clinical-stage biopharmaceutical company active in the discovery and development of T cells redirecting cancer immunotherapies. We use these powerful T cells to develop groundbreaking immunotherapies that target cancer cells. We are dedicated to transforming cancer treatment and improving patient outcomes through cutting-edge research and advanced TCR technology. The CRA II/Sr. will be responsible for ensuring clinical trial site management and monitoring activities in compliance with GCP guidelines, national and local regulations or laws, and SOPs. FLSA Classification: Hourly, Non-Exempt. Schedule: 8:00 AM – 5:00 PM; Monday to Friday. Reports to: Associate Director – Clinical Operations. Location: Remote. Responsibilities include supporting clinical trial site feasibility and site selection process; conducting all aspects of clinical monitoring for clinical trials including site qualification visits, site initiation visits, routine monitoring visits and close-out visits; supporting maintenance of Investigator Site Files and sponsor Trial Master Files; conducting site management as prescribed in clinical trial plans; preparing trip visit reports; reviewing clinical trial progress; organizing and presenting at Investigator Meetings; participating in development of Case Report Forms and clinical trial documents; acting as primary contact for clinical trial supplies and vendors; participating in clinical trial team meetings. Secondary functions include mentoring less experienced CRA colleagues, performing CTM tasks as delegated, and contributing to continuous improvement of Clinical Operation processes. Required experience includes a minimum Bachelor’s Degree preferably in life science or nursing, at least 4 years of on-site monitoring experience in pharmaceutical/biotechnology industry, in-depth knowledge of ICH-GCP, FDA and EMA regulations, understanding of medical oncology terminology, exceptional attention to detail, advanced presentation and organizational skills, and demonstrated computer skills including Microsoft Office and clinical trial systems. Preferred experience includes driving company standards and innovation, and fostering development in own expertise. Competencies include intermediate leadership skills, positive attitude, proficient time management, strong problem identification and communication skills, analytical reasoning, and project management skills. Work environment is remote with office setup requirements. Travel up to 75% is required. Legal eligibility to work in the United States is required. Immatics is an equal opportunity employer. Benefits include competitive health, dental, vision insurance, paid time off, paid holidays, employer-paid life insurance, disability coverage, 401(k) with company match, partially paid parental leave, and additional voluntary employee paid coverages. Professional growth opportunities with leading experts in T-cell immunotherapy and company provided learning and development opportunities.

By applying, you consent to your information being transmitted by Jooble to the Employer, as data controller, through the Employer’s data processor SonicJobs.
See Sonicjobs Privacy Policy at and Terms & Conditions at and SonicJobs Privacy Policy at and Terms of Use at

Job Tags

Similar Jobs