Senior Clinical Trials Operations Lead (Remote)

Immatics; Houston (TX); Remote; USD 95,000 - 120,000; Full time

Benefits offered by this job

Health Insurance

Vacation 4 weeks

Holidays (12 paid)

Parental leave

Life Insurance

Disability (short/long-term)

401(k) with company match

Job summary

Immatics, based in Houston, TX, seeks a Senior Clinical Trial Associate to support all stages of clinical trials, ensuring quality, compliance, and timely execution. This remote-friendly role collaborates with internal teams, CROs, and sites to drive trial activities and maintain essential documentation.

The position emphasizes CTMS/eTMF management, study start-up and closeout, and proactive problem-solving in a fast-paced environment. Competitive compensation and benefits are offered.

Qualifications

• Bachelor's degree in life sciences, nursing, or related field.
• 4+ years of clinical research experience with ICH-GCP knowledge.
• Experience supporting start-up, activation, maintenance and closeout activities.
• Ability to work in a fast-paced, collaborative environment.

Responsibilities

• Support trial start-up, activation, maintenance, and closeout activities.
• Maintain and quality-check trial information within CTMS, eTMF, and other systems.
• Coordinate with internal teams, CROs, vendors, and investigative sites.
• Assist with inspection and audit readiness and quality documentation.
• Schedule meetings, reviews, approvals, and administrative tasks.
• Manage study finances including PO issuance, invoices, and investigator payments.
• Support TMF/ISF maintenance and training tracking for study teams.
• Monitor site issues and data queries to help achieve milestones.
• Facilitate study communications and distribution of trial materials.

Skills

Problem solving

Independent work

Communication

Attention to detail

Education

Bachelor's degree in life sciences or related field

Tools

CTMS

eTMF

Job description

Immatics, based in Houston, TX, seeks a Senior Clinical Trial Associate to support all stages of clinical trials, ensuring quality, compliance, and timely execution. This remote-friendly role collaborates with internal teams, CROs, and sites to drive trial activities and maintain essential documentation.

The position emphasizes CTMS/eTMF management, study start-up and closeout, and proactive problem-solving in a fast-paced environment. Competitive compensation and benefits are offered.