Senior Clinical Trial Associate
<h3><strong>Who we are:</strong></h3>
<p>Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines that address critical health problems and have the potential to dramatically improve patients’ lives. Kymera is deploying TPD to address disease targets and pathways inaccessible with conventional therapeutics. Having advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions. Founded in 2016, Kymera has been recognized as one of Boston’s top workplaces for the past several years. For more information about our science, pipeline and people, please visit <a href="https://www.kymeratx.com" target="_blank">www.kymeratx.com</a> or follow us on <a href="https://twitter.com/KymeraTx?ref_src=twsrc%5Egoogle%7Ctwcamp%5Eserp%7Ctwgr%5Eauthor" target="_blank">X (formerly Twitter)</a> or <a href="http://www.linkedin.com/company/kymeratherapeutics" target="_blank">LinkedIn</a>. </p>
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<h3><strong>How we work:</strong></h3>
<ul>
<li><strong>PIONEER</strong>: We are courageous, resilient and rigorous in our mission to improve patients’ lives through our revolutionary degrader medicines.</li>
<li><strong>COLLABORATE</strong>: We value trust + transparency from everyone. Our goals are shared, our decisions data-driven and our camaraderie genuine.</li>
<li><strong>BELONG</strong>: We recognize our differences, inviting curiosity and inclusivity, so that our people are valued, seen, and heard.</li>
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<h3><strong>How you’ll make an impact:</strong></h3>
<p>The Senior Clinical Trial Associate (Sr. CTA) is responsible for supporting the Clinical Operations Team in the successful delivery of clinical trials in accordance with applicable regulations, within agreed timelines and budget. They are responsible for coordination, logistics, tracking, and administrative tasks in support of clinical trials from protocol concept through clinical study report.</p>
<ul>
<li>Collaborates with internal teams to support execution of Kymera-sponsored clinical trials</li>
<li>Assists with clinical operations oversight, including but not limited to, review of Monitoring Visit Reports, Study Plans and Essential Document Packets, etc.</li>
<li>Maintains eTMF in a state of inspection readiness through ongoing QC, reconciliation, and audit/inspection support to ensure compliance with GCP and regulatory requirements.</li>
<li>Ensures study issues and decision-related correspondence is maintained through the duration of the trial.</li>
<li>Maintains the Action Decision Issue Log and tracks actions to completion.</li>
<li>May contribute to development and review of study documents, including informed consent forms and study templates.</li>
<li>Performs reconciliations and tracking activities.</li>
<li>Manages a trial vendor with oversight.</li>
<li>Assists in the routing, tracking, and coordination of Site and CRO/Vendor Confidential Disclosure Agreements (CDAs) and other contracts with Clinical Operations, Legal, and Finance departments.</li>
<li>Leads eTMF archiving and coordinate file transfer and reconciliation with CROs at study closeout.</li>
<li>Maintains internal SharePoint site (folder creation, filing)</li>
<li>Drafts internal agendas and keeps meeting minutes; manages external partners in their execution of agendas and minutes.</li>
<li>Assists with logistics coordination for investigator meetings and external vendor meetings.</li>
<li>Participates in functional initiatives, including SOP development and review, staff training, and system/process improvement.</li>
<li>Develops and maintains strong, collaborative relationships with multiple cross-functional team members and external vendors.</li>
<li>Participate in co-monitoring visits as needed.</li>
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<h3><strong>Skills and experience you’ll bring:</strong></h3>
<ul>
<li>BS/BA degree; preference for a degree in a scientific or health related field</li>
<li>3+ years of experience in clinical trial execution, with at least one year of experience on the sponsor side.</li>
<li>Knowledge and understanding of the International Conference on Harmonization (ICH) and Good Clinical Practice (GCP) Guidelines.</li>
<li>Excellent communication (verbal and written), organizational, and problem-solving skills.</li>
<li>Experience building and managing external contract research relationships. </li>
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<div><em>Equal Employment Opportunity</em></div>
<p><span class="ui-provider a b c d e f g h i j k l m n o p q r s t u v w x y z ab ac ae af ag ah ai aj ak">Kymera Therapeutics is proud to be an equal opportunity employer, seeking to create a welcoming and diverse environment. All applicants will receive consideration for employment without regard to race, color, religion, creed, gender, national origin, age, disability, veteran status, pregnancy, sex, marital status, gender expression or identity, genetic information, sexual orientation, citizenship, or any other legally protected class.</span></p>
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<p><em><span class="ui-provider a b c d e f g h i j k l m n o p q r s t u v w x y z ab ac ae af ag ah ai aj ak">Compensation</span></em></p>
<ul>
<li>Kymera offers a competitive compensation package that recognizes both results and capabilities through market-based, performance-driven pay.</li>
<li>The anticipated base salary range for this role is $90,000 – $155,000, with eligibility for annual bonus, equity participation, and comprehensive benefits.</li>
<li>Actual salary is based on a holistic evaluation of the specific role/level as well as each candidate’s depth of experience and the capabilities they bring to the position.</li>
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