Clinical Trial Manager
$130k - $150kImmatics-US
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 Clinical Trial Manager (CTM) to support our U.S. Clinical Operations team. The CTM will oversee site management, monitoring oversight, and clinical trial operations activities to ensure compliance with GCP, regulatory requirements, and company SOPs. In this role, you will work closely with cross-functional teams and clinical sites to drive study execution, site engagement, and operational excellence across clinical trials.Reports to: Associate Director, Team Lead Site OperationsLocation: Fully RemoteSalary Range: $130,000 - $150,000Basic Qualifications:Bachelor’s degree in life sciences, nursing, or a related field2+ years of experience in on-site clinical monitoring and 2+ years of Clinical Trial Manager experience within the pharmaceutical or biotechnology industryStrong knowledge of ICH-GCP, FDA, EMA, and applicable clinical trial regulationsDemonstrated experience managing clinical trial sites, monitoring activities, and regulatory documentationProficiency with clinical trial systems and tools (e.g., CTMS, eTMF, Microsoft Office)Preferred Qualifications:Experience in oncology clinical trials or related therapeutic areasAdvanced ability to manage complex clinical operations processes and drive operational improvementsExperience leading training initiatives for CRAs and clinical trial sitesDemonstrated ability to drive quality, efficiency, and milestone achievement in fast-paced clinical environmentsExperience contributing to process harmonization, innovation, and continuous improvement initiativesStrong presentation, organizational, and cross-functional stakeholder management skillsIn this role you will:Partner with Clinical Operations leadership to support clinical trial execution and monitoring activities in alignment with project goalsLead site feasibility, selection, initiation, and greenlight activities for clinical trial sitesDevelop and maintain study-specific operational plans, training materials, and monitoring documentationOversee site management activities, including site engagement, regulatory submissions, and monitoring oversightReview trial progress, patient recruitment, and data quality metrics, and implement actions to support study objectivesProvide guidance and oversight to CRAs, including trip report review and training supportManage protocol and GCP deviations and contribute to continuous improvement of clinical operations processes and proceduresTravel required: up to 50% travel required, domestically and internationally.Qualified candidates will participate in a structured interview process, which includes:An initial recruiter phone screen (conducted via video)A recruiter-facilitated introduction and interview with the hiring leader and key stakeholders (via video)A final-stage interview, which may include an in-person meeting at our U.S. Headquarters in Houston, TXWhat 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 ImmaticsComprehensive Benefits:Competitive rates for Health, Dental, and Vision Insurance4 weeks of vacation, granted up front each year and prorated for first and last year of employment.12 company paid holidays7 days of sick time100% employer-paid life insurance up to at 1x annual salary, up to one hundred thousand dollars100% employer-paid short- and long-Term disability coverage401(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 OpportunityWe are an equal opportunity employer and are committed to building a diverse and inclusive workplace. We consider all qualified applicants for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, national origin, ancestry, age, marital status, disability, genetic information, veteran status, or any other status protected by applicable law.Reasonable AccommodationsWe are committed to providing reasonable accommodations to individuals with disabilities and to applicants with sincerely held religious beliefs, practices, or observances. If you require assistance or accommodation during the application or interview process, please contact us at View email address on click.appcast.io. #J-18808-Ljbffr Immatics-US
- ...Must have one of the following certifications: CCRC - Certified Clinical Research Coordinator (ACRP) or CCRP - Certified Clinical... ...workplace ESSENTIAL FUNCTIONS PEOPLE ESSENTIAL FUNCTIONS Performs management responsibilities of selection, scheduling, supervision, retention...SuggestedImmediate startFlexible hours
$130k - $150k
...in more than 50 cancers. Our cutting-edge science and robust clinical pipeline form the broadest PRAME franchise with the most PRAME... ...on patients globally.Role Overview:We are seeking a Clinical Trial Manager (CTM) to support our U.S. Clinical Operations team. The CTM...SuggestedTemporary workWork at officeImmediate start- ...technology company advancing the diagnosis and management of coronary artery disease using cutting... .... Responsibilities Participate in clinical research activities at the study and... ...and project management tasks. Develop trial timelines, enrollment projections, and instructional...Suggested
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...Consultants - Memorial CityPay Range:$49,608.00 - $87,276.80Position SummaryThe Clinical Research Coordinator functions as an integral part of the Research Team in clinical trial management at Oncology Consultants. The Clinical Research Coordinator is involved in multiple...Suggested- ...Position Clinical Research Coordinator II Location Juno Research, Houston, TX Department Study Operations... ...successful execution of multiple concurrent clinical trials through effective study coordination, subject management, and cross‑functional communication. This...SuggestedWork experience placement
$19.66 - $34.59 per hour
...supervision of the Principal Investigator. The Clinical Research Coordinator I (non-RN) is... ...successful implementation and ongoing management of the research studies. Ability to perform... ...(phase 4, observational/registry trial design) and associated study procedures....Contract workRemote workMonday to Friday- Immatics US, Inc. is seeking a Clinical Trial Manager to support the U.S. Clinical Operations team. The role focuses on overseeing clinical trial activities to ensure compliance with regulatory requirements. You will work closely with clinical sites to drive operational...Remote job
- ...accommodation or an alternative application process. Clinical Research Coordinator (CRC)-FT Full Time HDR... ...responsible for the overall coordination, organization, management, and efficient implementation of clinical trials. The CRC II completes all study related procedures...Full timeWork at office
- ...service focus and positive language principles. Sufficient clinical and research data entry skills. Capability to handle challenging... ...report forms, electronic data capture portals, and clinical trial management system following established procedures. Quality/Safety...
- ...Research Coordinator I to oversee day-to-day activities of IBD clinical trials. This full-time, on-site position collaborates with a team... ...compliance and successful study execution. The candidate will manage IRB submissions, data collection, and patient recruitment through...Full time
- ...Clinical Research Coordinator I Position is on-site Monday - Friday in South Houston, Texas Renal Specialists of Houston 3333... ...accountability logs readily available. Ongoing Study oversight and management: Plan subject visits according to protocol specific visit...Contract workLocal areaMonday to FridayNight shift
- ...Employee Type: Non-Exempt - FT Job Title: Clinical Research Coordinator II FSLA... ...: Non-Exempt Reports to: Site Operations Manager Job Summary / Objective The Clinical Research... ...the management and oversight of clinical trials. This role involves working closely with...Work at officeMonday to Friday
- ...Location: CyFair - Houston, TX 77065 The Clinical Research Coordinator III will ensure... ...Standards with all the relevant clinical trial documentation. Completing and overseeing... ...staff. Any other matters as assigned by management. KNOWLEDGE & EXPERIENCE Education: High...
- ...Clinical Research Coordinator II - Houston, TX Houston, TX Iterative Health is a healthcare... ...cardiology. By combining deep clinical trial expertise with cutting-edge AI, we... ...guidelines. This role is responsible for managing complex studies with minimal oversight while...Work at office
- ...of related research experience. The role demands strong communication and analytical skills. Responsibilities include maintaining clinical study records, scheduling patient appointments, and ensuring regulatory compliance. This position requires significant collaboration...
- ...the other departments within Emerus. The PM is responsible for managing two categories of projects: Hospital Openings and Enterprise. Hospital... ...preferred Bachelor's Degree or higher required PMP required Clinical licensure or relevant clinical credential required (e.g. RN,...Temporary work
$20 - $25 per hour
...Clinical Research Data Coordinator - Oncology Onsite Contract Required Qualifications MUST HAVE 3 years of clinical... ...or III studies MUST HAVE experience with: Clinical trial data entry and management Query resolution Electronic Data Capture (EDC)...Contract workTemporary work- Houston Methodist is seeking a qualified leader to manage department operations in Houston. This role requires a Bachelor's in a relevant... ...in healthcare (one in management), and a certification as a Clinical Research Coordinator. Responsibilities include overseeing...
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- ...Bachelor's degree and four years of research experience. The ideal candidate will also have skills in patient communication, data management, and the ability to work independently. In this role, you will coordinate studies and manage participant data effectively,...
- ...Research Data Coordinator to provide administrative and patient care services for coordinating research studies. You will collect and manage patient data, coordinate protocol administration, and ensure regulatory compliance within a hybrid Texas Medical Center setting....
- Houston Methodist is looking for a Research Coordinator in Houston, Texas. The successful candidate will coordinate daily activities of research protocols, assess patient qualifications for studies, and ensure data accuracy and safety of research participants. Qualified...
- ...Senior Clinical Research Coordinator Are you passionate about the patient experience? At HCA Healthcare, we are committed to caring... ...meetings, etc.) Able to guide research team members on the management of non-compliant data and/or study activities Monitor patient...Temporary workLocal areaFlexible hours
- Houston Methodist is seeking a Research Coordinator to manage day-to-day activities of research protocols, assess patient eligibility... ...guidelines, and reliable communication to support compliant, efficient clinical studies. Strong attention to detail and organizational skills...
- Dm Clinical Research Group is seeking a Clinical Research Coordinator III in Houston, Texas. This role involves ensuring quality research is conducted at investigative sites, adhering to sponsor protocols, FDA regulations, and guidelines. The successful candidate will...
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