Senior Clinical Research Associate

<p><b><i>J</i><i><span style="overflow-wrap: break-word; display: inline; text-decoration: inherit; hyphens: auto;">oin Immatics and shape</span> the future <span style="overflow-wrap: break-word; display: inline; text-decoration: inherit; hyphens: auto;">of cancer immunotherapy</span></i><i>; one patient at a time! </i></b><span> </span></p><p></p><p><span>Immatics is committed to making a meaningful impact on the lives of patients with cancer. We are the global leader in precision targeting of </span><b>PRAME</b><span>, a target expressed in more than 50 cancers. <span style="overflow-wrap: break-word; display: inline; text-decoration: inherit; hyphens: auto;">Our cutting-edge science</span> and robust clinical pipeline form the broadest </span><b>PRAME</b><span> franchise with the most </span><b>PRAME</b><span> indications and modalities, spanning TCR T-cell therapies and <span style="overflow-wrap: break-word; display: inline; text-decoration: inherit; hyphens: auto;">TCR bispecifics. </span></span></p><p><span> </span></p><p><b>Why Join Us?</b><span> </span></p><ul><li><p><b>Innovative <span style="overflow-wrap: break-word; display: inline; text-decoration: inherit; hyphens: auto;">Environment:  </span></b><span><span style="overflow-wrap: break-word; display: inline; text-decoration: inherit; hyphens: auto;">Help to pioneer advancements in</span> cancer immunotherapy. </span></p></li><li><p><b>Collaborative Culture:</b><span> Be part of </span><span>a diverse team dedicated to your <span style="overflow-wrap: break-word; display: inline; text-decoration: inherit; hyphens: auto;">professional growth. </span></span></p></li><li><p><b>Global Impact:  </b><span>Contribute to therapies <span style="overflow-wrap: break-word; display: inline; text-decoration: inherit; hyphens: auto;">that make a lasting</span> <span style="overflow-wrap: break-word; display: inline; text-decoration: inherit; hyphens: auto;">impact on patients globally. </span></span></p></li></ul><p><span> </span></p><p><b>Role Overview:</b><span> </span></p><p><span>We are seeking a Senior Clinical Research Associate (CRA) to support our Clinical Operations team. The Senior CRA will be responsible for overseeing clinical trial site management and monitoring activities to ensure compliance with ICH-GCP, regulatory requirements, and company SOPs. In this role, you will partner closely with clinical sites and cross-functional teams to support high-quality study execution, patient recruitment, and operational excellence across clinical trials. </span></p><p><span> </span><span> </span></p><p><b>Reports to</b><span>: Associate Director, Team Lead Site Operations</span><span> </span></p><p><b>Location</b><span style="overflow-wrap: break-word; display: inline; text-decoration: inherit; hyphens: auto;">: Fully Remote </span></p><p><b>Salary Range:</b> $120,000 to $135,000 </p><p></p><p><b>Basic Qualifications:</b> </p><ul><li><p><span>Bachelor’s degree in life sciences, nursing, or a related field  </span></p></li><li><p><span>4+ years of on-site monitoring experience within the pharmaceutical or biotechnology industry, including all clinical monitoring visit types  </span></p></li><li><p><span>Strong knowledge of ICH-GCP, FDA, EMA, and applicable clinical trial <span style="overflow-wrap: break-word; display: inline; text-decoration: inherit; hyphens: auto;">regulations  </span></span></p></li><li><p><span>Demonstrated experience managing clinical trial <span style="overflow-wrap: break-word; display: inline; text-decoration: inherit; hyphens: auto;">sites, monitoring activities,</span> and clinical trial <span style="overflow-wrap: break-word; display: inline; text-decoration: inherit; hyphens: auto;">documentation  </span></span></p></li><li><p><span><span style="overflow-wrap: break-word; display: inline; text-decoration: inherit; hyphens: auto;">Proficiency with</span> clinical trial systems and tools (e.g., CTMS, eTMF, Microsoft Office) </span></p></li></ul><p></p><p><b><span style="overflow-wrap: break-word; display: inline; text-decoration: inherit; hyphens: auto;">Preferred Qualifications: </span></b> </p><ul><li><p><span>Experience in oncology clinical trials or related therapeutic areas  </span></p></li><li><p><span>Advanced presentation, organizational, and stakeholder management skills  </span></p></li><li><p><span>Experience mentoring or training junior CRAs and supporting cross-functional clinical operations <span style="overflow-wrap: break-word; display: inline; text-decoration: inherit; hyphens: auto;">activities  </span></span></p></li><li><p><span>Demonstrated ability to drive quality, efficiency, and continuous improvement initiatives in clinical <span style="overflow-wrap: break-word; display: inline; text-decoration: inherit; hyphens: auto;">operations  </span></span></p></li><li><p><span>Strong understanding of clinical trial recruitment strategies, data capture, and site engagement best <span style="overflow-wrap: break-word; display: inline; text-decoration: inherit; hyphens: auto;">practices  </span></span></p></li><li><p><span>Experience contributing to global harmonization, process optimization, or operational innovation initiatives </span></p></li></ul><p></p><p><b>In this role you will:</b> </p><ul><li><p><span>Conduct all clinical monitoring activities, including site qualification, initiation, routine monitoring, and close-out visits  </span></p></li><li><p><span>Support site feasibility, site selection, and ongoing site management activities throughout the clinical trial <span style="overflow-wrap: break-word; display: inline; text-decoration: inherit; hyphens: auto;">lifecycle  </span></span></p></li><li><p><span>Review clinical trial progress, patient recruitment, and data quality metrics, and implement actions to support study <span style="overflow-wrap: break-word; display: inline; text-decoration: inherit; hyphens: auto;">objectives  </span></span></p></li><li><p><span><span style="overflow-wrap: break-word; display: inline; text-decoration: inherit; hyphens: auto;">Maintain accurate and timely monitoring</span> documentation, including trip reports and trial master file records  </span></p></li><li><p><span>Collaborate with vendors, clinical sites, and cross-functional teams to support study execution and operational <span style="overflow-wrap: break-word; display: inline; text-decoration: inherit; hyphens: auto;">compliance  </span></span></p></li><li><p><span>Participate in investigator meetings, clinical trial documentation development, and study team meetings  </span></p></li><li><p><span>Mentor junior CRA team members and contribute to continuous improvement of clinical operations processes and procedures </span></p></li></ul><p></p><p><b>Travel required: </b>Willingness to travel up to 75%. Valid Driver's License <span style="overflow-wrap: break-word; display: inline; text-decoration: inherit; hyphens: auto;">preferable.  </span></p><p></p><p><b>Qualified candidates <span style="overflow-wrap: break-word; display: inline; text-decoration: inherit; hyphens: auto;">will participate in</span> a structured interview process, which includes:</b> </p><ul><li><p><span>An <span style="overflow-wrap: break-word; display: inline; text-decoration: inherit; hyphens: auto;">initial recruiter</span> phone screen (conducted via video) </span></p></li><li><p><span>A <span style="overflow-wrap: break-word; display: inline; text-decoration: inherit; hyphens: auto;">recruiter-facilitated</span> introduction and interview with the hiring leader and key stakeholders (via video) </span></p></li><li><p><span>A final-stage interview, which may include an in-person meeting at our U.S. Headquarters in Houston, TX </span></p></li></ul><p></p><p><b>What do we offer?</b>  </p><p>At Immatics, we believe in investing in our team’s <span style="overflow-wrap: break-word; display: inline; text-decoration: inherit; hyphens: auto;">health, safety and</span> <span style="overflow-wrap: break-word; display: inline; text-decoration: inherit; hyphens: auto;">well-being. Here’s what</span> you can expect if <span style="overflow-wrap: break-word; display: inline; text-decoration: inherit; hyphens: auto;">you join Immatics </span></p><p>  </p><p><b>Comprehensive Benefits</b>:  </p><ul><li><p><span>Competitive rates for Health, Dental, and Vision Insurance </span></p></li><li><p><span>4 weeks <span style="overflow-wrap: break-word; display: inline; text-decoration: inherit; hyphens: auto;">of vacation, granted</span> up front each year and prorated for first and last year <span style="overflow-wrap: break-word; display: inline; text-decoration: inherit; hyphens: auto;">of employment. </span></span></p></li><li><p><span>12 company paid holidays </span></p></li><li><p><span>7 days of sick time </span></p></li><li><p><span><span style="overflow-wrap: break-word; display: inline; text-decoration: inherit; hyphens: auto;">100% employer-paid life insurance</span> up to at 1x annual salary, up to one hundred thousand dollars  </span></p></li><li><p><span><span style="overflow-wrap: break-word; display: inline; text-decoration: inherit; hyphens: auto;">100% employer-paid short-</span> <span style="overflow-wrap: break-word; display: inline; text-decoration: inherit; hyphens: auto;">and long-Term disability coverage</span>  </span></p></li><li><p><span>401(k) <span style="overflow-wrap: break-word; display: inline; text-decoration: inherit; hyphens: auto;">with immediate eligibility</span> and company match… </span></p><ul><li><p><span>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. </span></p></li></ul></li><li><p><span><span style="overflow-wrap: break-word; display: inline; text-decoration: inherit; hyphens: auto;">Partially paid parental leave</span> for eligible employees. </span></p></li><li><p><span><span style="overflow-wrap: break-word; display: inline; text-decoration: inherit; hyphens: auto;">Additional voluntary</span> <span style="overflow-wrap: break-word; display: inline; text-decoration: inherit; hyphens: auto;">employee-paid benefits</span> and <span style="overflow-wrap: break-word; display: inline; text-decoration: inherit; hyphens: auto;">services, including accident, hospital indemnity,</span> <span style="overflow-wrap: break-word; display: inline; text-decoration: inherit; hyphens: auto;">and critical illness insurance,</span> as well as <span style="overflow-wrap: break-word; display: inline; text-decoration: inherit; hyphens: auto;">identity theft protection</span> <span style="overflow-wrap: break-word; display: inline; text-decoration: inherit; hyphens: auto;">and pet insurance.  </span></span></p></li></ul><p><span style="color:#000000"><b>Equal Employment Opportunity</b> </span></p><p style="color:!important"><span style="color:#000000">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.   </span></p><p style="color:!important"><span style="color:#000000"> </span></p><p style="color:!important"><span style="color:#000000"><b>Reasonable Accommodations </b></span></p><p style="color:!important"><span style="color:#000000">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 </span><a href="mailto:RecruitingUS@immatics.com" target="_blank" rel="noopener noreferrer"><span style="color:#467886"><u><span style="overflow-wrap: break-word; display: inline; text-decoration: inherit; hyphens: auto;">RecruitingUS@immatics.com</span></u></span></a>.   </p><p style="color:!important"><span style="color:#000000"> </span></p><p style="color:!important"><span style="color:#000000"><b>Work Authorization</b> </span></p><p style="color:!important"><span style="color:#000000">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. </span></p><p style="color:!important"><span style="color:#000000"> </span></p><p style="color:!important"><span style="color:#000000"><b>Pre-Employment Requirements</b> </span></p><p style="color:!important"><span style="color:#000000">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.   </span></p>

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