Job Description

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

Immatics is at the forefront of immunotherapy innovation, working to harness the power of T cells to transform cancer treatment.

Immatics is an exceptional clinical-stage biopharmaceutical company active in the discovery and development of T cells redirecting cancer immunotherapies. We use these powerful T cells to develop groundbreaking immunotherapies that target cancer cells. We are dedicated to transforming cancer treatment and improving patient outcomes through cutting-edge research and advanced TCR technology.

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.

We are seeking a Medical Monitor to support our Clinical Development team. The Medical Monitor will serve as the key clinical expert for ongoing clinical trials, providing medical oversight, supporting safety monitoring activities, and performing medical data reviews to ensure both patient safety and data integrity.

FLSA Classification : Salary, Exempt
Schedule : 8:00 AM - 5:00 PM; Monday to Friday; Hours are flexible
Reports to : SVP, Clinical Development
Location : Fully Remote

What You'll Do:

As a Medical Monitor , you will play a key role in supporting our Clinical Development operations:

• Medical and Safety Oversight

• Provide medical oversight for clinical trials from Phase 1 to Phase 3.

• In collaboration with Drug Safety, assess (Serious) Adverse Events with regards to causality, expectedness and clinical management- including CIOMS and MedWatch forms

• Serve as primary contact for medical investigator enquiries

• Reviews MPs and other documents related to safety data review

• Lead/support medical data review meetings, DSMB meeting and other meetings related to patient safety

• Collaborate with Drug Safety on signal detection

• Trial conduct and Protocol Compliance

• Provide medical input on trial design and clinical trial protocol development/amendments

• Review and approve eCRFs

• Provide input for Investigator Brochures

• Ensure eligibility criteria, IMP dosing and management of adverse events, and safety assessments are in line with the clinical trial protocol

• Participate in Protocol Deviation assessments

• Support investigators by addressing protocol-related questions

• Participate in site selection and trainings (e.g. SIVs)

• Contribute to Investigator Meetings and all types of site visits as needed

• Regulatory

• Support regulatory filings and responses to regulatory enquiries

• Provide medical expertise for Risk Management Plans

• Data review, analysis and interpretation

• Ensure timely medical review of individual and aggregate safety and efficacy data

• Review patient narratives

• Contribute to interpretation of data in early clinical trials

• Contribute to clinical study reports, publications and presentations

Required Experience and Education :

• MD PhD in Biomedical Sciences, or a related field

• Prior Experience as a Medical Monitor

• Experience in Oncology

Preferred Experience and Education:

• Advanced experience in cell therapy, including clinical development or trial oversight

Comp etencies:

• Initiative

• Problem Solving

• Critical Thinking

• Interpersonal Communication

• Attention to Detail

Work Environment:

As a remote medical monitor, the work environment is primarily home-based, requiring a dedicated and well-organized workspace that supports focused, uninterrupted work. The role involves frequent communication with clinical trial sites, sponsors, and cross-functional teams via email, video conferencing, and phone calls. Despite working remotely, the medical monitor plays a critical role in overseeing the safety and integrity of clinical trials, reviewing patient data, assessing adverse events, and providing medical guidance in real time. This position demands strong self-discipline, excellent time management skills, and the ability to collaborate effectively across multiple time zones and geographies, ensuring that clinical oversight remains consistent and compliant with regulatory standards.

Travel required: Up to 20% travel will be required, mostly in the US and occasionally internationally

Physical demands:

• Communicating Verbally - expressing or exchanging ideas by means of the spoken word to impart oral information to others to convey detailed spoken instructions or other workers accurately, loudly or quickly.

• Hearing - the ability to hear, understand, and distinguish speech and/or other sounds one-on-one, group or conference, telephone, and other sounds.

• Keyboarding - entering data or text into a computer or other machine by means of a keyboard. Devices include a traditional keyboard, 10 key-pad, touch screens and others.

• Lifting - raising or lowering an object (up to 25 lbs) from one level to another (includes upward pulling). Carrying is to transport an object - usually by holding it in the hands or arms but may occur on the shoulder.

• Near Visual Acuity - clarity of vision at approximately 20 inches or less (working with small objects, reading small print, including the use of computers).

• Pushing - Exerting force upon an object so that the object moves away from the object.

• Pulling - Exerting force upon an object so that the object moves toward the force.

• Sitting - remaining in a sitting position for at least 50% of the time.

• Standing/Walking - remain on one's feet in an upright position at a workstation.

• Stooping - occasional bending the body downward and forward by bending the spine at the waist - requiring full use of the lower extremities and back muscles.

Work authorization/security clearance requirements :

Legal eligibility to work in the United States is required. Immatics participates in E-Verify and all new employees will be subject to the Department of Homeland Security requirements for employment.

Affirmative Action/EEO statement :

Immatics is an equal opportunity employer. All employment decisions including the decision to hire, promote, discipline, or discharge, will be based on merit, competence, performance, and business needs.

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

Comprehensive Benefits :

• Competitive rates for Health, Dental, and Vision Insurance

• 4 weeks of Paid Time off, granted up front each year and prorated for first and last year of employment.

• Sick Time Off - 56 hours

• 12 Paid Holidays

• 100% Employer-Paid Life Insurance up to at 1x annual salary, up to 100K ( club together)

• 100% Employer Paid Short- and Long-Term Disability Coverage

• 401(k) with Immediate Eligibility & company match...

• You are eligible for 401(k) plan participation as of your first paycheck.

• 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. (3 weeks)

• Additional voluntary employee paid coverages including Accident, Hospital Indemnity, and Critical Illness Employee Paid Identity Theft Protection and Pet Insurance.

Professional Growth :

• Opportunities to work with leading experts in the field of T-cell immunotherapy.

• Company provided learning and development opportunities

• Fast paced, high demand collaborative and dynamic environment.

Immatics NV

Job Tags

Temporary work, Immediate start, Remote work, Work from home, Flexible hours, Monday to Friday,

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