[Hiring] Senior Clinical Trial Associate @Immatics

Role Description

We are seeking a highly organized and proactive Senior Clinical Trial Associate (CTA) to join our Clinical Operations team. In this pivotal role, you will help drive the successful execution of clinical trials by providing critical operational and administrative support, ensuring studies are conducted efficiently, compliantly, and with the highest standards of quality.

Qualifications

• Bachelor’s degree in life sciences, nursing, or a related field
• 4+ years’ working experience in the clinical research area in the Pharmaceutical or Biotech industry with ICH-GCP knowledge, or equivalent

Requirements

• Strong problem-solving skills with the ability to analyze issues, identify root causes, and implement effective solutions.
• Self-motivated and able to work independently in a fast-paced environment.
• Strong understanding of clinical trial processes and interconnected operational workflows.
• Continuous improvement mindset with a passion for enhancing processes and team effectiveness.
• Demonstrated ability to drive innovation and share expertise across teams.

Responsibilities

• Support clinical trial start-up, activation, maintenance, and closeout activities, ensuring timely collection and management of essential study documents.
• Maintain and perform quality reviews of trial information within CTMS, eTMF, and other clinical systems.
• Partner with internal teams, CROs, vendors, and investigative sites to drive study execution and resolve operational issues.
• Support inspection and audit readiness through accurate, complete, and compliant trial documentation.
• Coordinate trial-related meetings, documentation reviews, approvals, and key administrative activities.
• Manage purchase orders, invoices, investigator payments, and study-related financial tracking.
• Prepare, review, and quality-check study documents, reports, trackers, and investigator site files.
• Support TMF and ISF maintenance, reconciliation, and quality oversight to ensure ongoing compliance.
• Coordinate training assignments, system access, and compliance tracking for study teams.
• Monitor site issues, action items, and data query resolution to support study milestones.
• Support tracking and follow-up of outstanding EDC queries and facilitate timely resolution by appropriate study team members and/or sites.
• Facilitate site communications, including study updates, newsletters, and distribution of trial materials.
• Contribute to risk identification, issue escalation, process improvements, and inspection readiness efforts.
• Support the development of SOPs, work instructions, guidance documents, and training materials.
• May assist with remote and on-site monitoring activities, as appropriate.

Travel Requirements

• Optional travelling for business reasons

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.