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Clinical Trial Manager

Role overview

Qualifications

  • Bachelor’s degree in life sciences, nursing, or a related field
  • 2+ years of experience in on-site clinical monitoring
  • 2+ years of Clinical Trial Manager experience within the pharmaceutical or biotechnology industry
  • Strong knowledge of ICH-GCP, FDA, EMA, and applicable clinical trial regulations

Responsibilities

  • Partner with Clinical Operations leadership to support clinical trial execution and monitoring activities in alignment with project goals
  • Lead site feasibility, selection, initiation, and greenlight activities for clinical trial sites
  • Develop and maintain study-specific operational plans, training materials, and monitoring documentation
  • Oversee site management activities, including site engagement, regulatory submissions, and monitoring oversight

Key facts

  • Remote from: United States
  • Full time
  • Mid-level (2-5 years)
  • 192 - 192K yearly
  • English

Other skills

  • Microsoft Office
  • Training And Development
  • Communication
  • Organizational Skills

About the company

BioHouston logo

BioHouston

Non-profit Organizations

BioHouston, Inc. is a non-profit, tax-exempt [501(c)(3)] corporation founded by Houston-region academic/research institutions. We are leading a broad effort to establish the Houston region as a vigorous global competitor in life science and biotechnology commercialization. Our mission is to create an environment that will stimulate technology transfer and research commercialization, thereby generating economic wealth for the Houston region and making it a global competitor in life science commercialization. BioHouston's activities provide the greatest leverage in making the Houston region a world-class competitor in the life science industry. All of our activities are designed to: CONVENE people and organizations that need to come together to make the life science industry in Houston ignite, including scientists, intellectual property and product development experts, venture capitalists, pharmaceutical companies, and others COMMUNICATE and interact so that people and organizations can learn from one another, share information and explore opportunities CATALYZE the discoveries and commercial development so that the true potential of the life science industry in Houston can be unlocked.

Company details

IndustryNon-profit Organizations
Company size2 - 10

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Job description

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 Operations   
Location: Fully Remote 

Salary Range: $130,000 - $150,000 

Basic Qualifications:  

  • Bachelor’s degree in life sciences, nursing, or a related field  

  • 2+ years of experience in on-site clinical monitoring and 2+ years of Clinical Trial Manager experience within the pharmaceutical or biotechnology industry  

  • Strong knowledge of ICH-GCP, FDA, EMA, and applicable clinical trial regulations  

  • Demonstrated experience managing clinical trial sites, monitoring activities, and regulatory documentation  

  • Proficiency with clinical trial systems and tools (e.g., CTMS, eTMF, Microsoft Office) 

Preferred Qualifications:  

  • Experience in oncology clinical trials or related therapeutic areas  

  • Advanced ability to manage complex clinical operations processes and drive operational improvements  

  • Experience leading training initiatives for CRAs and clinical trial sites  

  • Demonstrated ability to drive quality, efficiency, and milestone achievement in fast-paced clinical environments  

  • Experience contributing to process harmonization, innovation, and continuous improvement initiatives  

  • Strong presentation, organizational, and cross-functional stakeholder management skills 

In this role you will: 

  • Partner with Clinical Operations leadership to support clinical trial execution and monitoring activities in alignment with project goals  

  • Lead site feasibility, selection, initiation, and greenlight activities for clinical trial sites  

  • Develop and maintain study-specific operational plans, training materials, and monitoring documentation  

  • Oversee site management activities, including site engagement, regulatory submissions, and monitoring oversight  

  • Review trial progress, patient recruitment, and data quality metrics, and implement actions to support study objectives  

  • Provide guidance and oversight to CRAs, including trip report review and training support  

  • Manage protocol and GCP deviations and contribute to continuous improvement of clinical operations processes and procedures 

Travel 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, TX 

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 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.  

Equal Employment Opportunity

We 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 Accommodations 

We 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 RecruitingUS@immatics.com.   

Work Authorization

Applicants must be authorized to work in the United States without the need for current or future sponsorship.  Visa sponsorships may be available for certain roles. 

Pre-Employment Requirements

Employment is contingent upon successful completion of a background check, reference checks and pre-employment drug screening, where permitted by applicable law.  For certain roles, additional screenings such as a credit check or motor vehicle record review may be required, where job-related and consistent with business necessity.   

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MR

Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
linkedin.com/in/marcusrivera
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