Note: The job is a remote job and is open to candidates in USA. Immatics is a biotechnology company focused on cancer immunotherapy and precision targeting. The Senior Clinical Research Associate will oversee clinical trial site management and monitoring activities, ensuring compliance with ICH-GCP, regulatory requirements, and company SOPs. The role supports site engagement, patient recruitment, documentation, cross-functional study execution, and operational excellence.
Responsibilities
- Conduct all clinical monitoring activities, including site qualification, initiation, routine monitoring, and close-out visits
- Support site feasibility, site selection, and ongoing site management activities throughout the clinical trial lifecycle
- Review clinical trial progress, patient recruitment, and data quality metrics, and implement actions to support study objectives
- Maintain accurate and timely monitoring documentation, including trip reports and trial master file records
- Collaborate with vendors, clinical sites, and cross-functional teams to support study execution and operational compliance
- Participate in investigator meetings, clinical trial documentation development, and study team meetings
- Mentor junior CRA team members and contribute to continuous improvement of clinical operations processes and procedures
Skills
- Bachelor's degree in life sciences, nursing, or a related field
- 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)
- Willingness to travel up to 75%
- Applicants must be authorized to work in the United States without the need for current or future sponsorship
- Experience in oncology clinical trials or related therapeutic areas
- Advanced presentation, organizational, and stakeholder management skills
- Experience mentoring or training junior CRAs and supporting cross-functional clinical operations activities
- Demonstrated ability to drive quality, efficiency, and continuous improvement initiatives in clinical operations
- Strong understanding of clinical trial recruitment strategies, data capture, and site engagement best practices
- Experience contributing to global harmonization, process optimization, or operational innovation initiatives
- Valid Driver's License preferable
Benefits
- Competitive rates for Health, Dental, and Vision Insurance
- 4 weeks of vacation, granted up front each year and prorated for first and last year of employment.
- 12 company paid holidays
- 7 days of sick time
- 100% employer-paid life insurance up to at 1x annual salary, up to one hundred thousand dollars
- 100% employer-paid short- and long-Term disability coverage
- 401(k) with immediate eligibility and company match. The company will match 100% of your contributions up to 3% of your base salary for the first two years of employment, 4% for years 2-3 of employment, and up to 5% of your salary from the fourth year onward of continued employment.
- Partially paid parental leave for eligible employees.
- Additional voluntary employee-paid benefits and services, including accident, hospital indemnity, and critical illness insurance, as well as identity theft protection and pet insurance.
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