Senior Clinical Sciences Manager

Immatics

Senior Clinical Sciences Manager supporting the execution of clinical trials at Immatics. Handling patient journey navigation and collaborating on clinical trial materials and protocols.

Posted 4/29/2026full-timeRemote • Texas • 🇺🇸 United StatesSenior💰 $155,000 - $175,000 per yearWebsite

About the role

Key responsibilities & impact

Support the execution of our clinical trials, including the SUPRAME (IMA203-301) study.
Responsible for supporting patient journey navigation, primarily for U.S. sites.
Update patient-facing and clinical trial materials.
Contribute to protocol development.
Conduct literature research.
Support trial outcome reporting.
Deliver training to internal and external stakeholders.
Serve as a key point of contact for clinical trial protocol and patient-facing material inquiries from sites and internal teams.
Support patient journey navigation, including proactive management of screening activities.
Contribute to authoring and updating clinical trial documents, including protocols, reports, and investigator materials.
Support preparation of responses for IRBs and regulatory authorities.
Deliver site training on clinical trial protocols and patient-facing materials (e.g., SIVs).
Maintain accurate eTMF documentation and filing.
Travel required: up to 20% travel required , domestically and internationally.

Requirements

What you’ll need

Bachelor’s degree in biology, pharmacy, or a related scientific field
7+ years of experience conducting literature research using clinical and medical databases
Demonstrated experience supporting clinical trial activities, including protocol and patient-facing materials
Experience training site staff or internal teams on clinical trial protocols and materials
Master’s degree in biology, pharmacy, or a related scientific field (preferred)
Experience supporting regulatory documentation (e.g., IRB submissions, RFIs) (preferred)
Experience working in oncology or cell therapy clinical development (preferred)
Advanced ability to translate complex scientific data into clear, actionable insights and presentations (preferred)
Experience working cross-functionally in a global clinical trial environment (preferred)

Benefits

Comp & perks

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.

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

clinical trial executionprotocol developmentliterature researchclinical trial documentationeTMF documentationregulatory documentationIRB submissionspatient journey navigationscreening activitiestraining delivery

Soft Skills

communicationorganizationalcross-functional collaborationstakeholder engagementpresentation skillsproactive managementproblem-solvingattention to detailadaptabilityleadership