Remote Senior CTA Trials Operations

Immatics US

United States

Remote

USD 95,000 - 120,000

Full time

5 days ago
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Benefits offered by this job

Health insurance
Vacation
Holidays
Sick leave
Life insurance
Disability insurance
401(k) matching
Parental leave
Pet insurance

Job summary

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.

Qualifications

  • 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.

Responsibilities

  • 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.

Skills

Problem-solving
Independent work
Clinical trial processes
Process improvement
Cross-team collaboration

Education

Bachelor's degree in life sciences

Tools

CTMS
eTMF

Job description

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.

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