Senior Clinical Trial Associate

Immatics US; United States; A distancia; USD 95.000 - 120.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Health insurance

Vacation

Holidays

Sick leave

Life insurance

Disability insurance

401(k) matching

Parental leave

Pet insurance

Descripción de la vacante

Immatics US is seeking a Senior Clinical Trial Associate to join our Clinical Operations team. You will drive trial execution by delivering operational support, ensuring compliance, and maintaining high-quality study documentation.

Reporting to the Associate Director, Team Lead Site Operations, this remote US role requires 4+ years in clinical research and solid ICH-GCP knowledge. Join us to advance cancer immunotherapy and patient outcomes.

Formación

• Bachelor's degree in life sciences, nursing, or related field.
• 4+ years' experience in clinical research in Pharma/Biotech with ICH-GCP knowledge.
• Strong problem-solving and analytical skills.
• Ability to work independently in a fast-paced environment.

Responsabilidades

• Support clinical trial start-up, activation, maintenance, and closeout activities with timely collection of essential study documents.
• Maintain and perform quality reviews of trial information within CTMS, eTMF, and other systems.
• Partner with internal teams, CROs, vendors, and sites to drive study execution and resolve issues.
• Support inspection and audit readiness through accurate, compliant trial documentation.
• Coordinate trial-related meetings, documentation reviews, approvals, and administrative activities.
• Manage purchase orders, invoices, investigator payments, and study-related financial tracking.

Conocimientos

Problem-solving

Independent work

Clinical trial processes

Process improvement

Cross-team collaboration

Educación

Bachelor's degree in life sciences

Herramientas

CTMS

eTMF

Descripción del empleo

Join Immatics and shape the future of cancer immunotherapy; one patient at a time!

Immatics is committed to making a meaningful impact on the lives of patients with cancer. We are the global leader in precision targeting of PRAME , a target expressed in more than 50 cancers. Our cutting-edge science and robust clinical pipeline form the broadest PRAME franchise with the most PRAME indications and modalities, spanning TCR T-cell therapies and TCR bispecifics.

Why Join Us?

Innovative Environment: Help to pioneer advancements in cancer immunotherapy.

Collaborative Culture: Be part of a diverse team dedicated to your professional growth.

Global Impact: Contribute to therapies that make a lasting impact on patients globally.

Role Overview

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.

Reports to: Associate Director, Team Lead Site Operations

Location: US, Fully Remote

Salary Range: $95,000 to $120,000

Basic 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

Preferred Qualifications

• 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.

In this role you will:

• 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

Qualified candidates will participate in a structured interview process, which includes:

An initial recruiter phone screen (conducted via video)

Interviews with the hiring leader and other key stakeholders (via video)

A final-stage interview

What do we offer?

At Immatics, we believe in investing in our team's health, safety and well-being. Here's what you can expect if you join Immatics

• 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.

Equal Employment Opportunity

We are an equal opportunity employer and