<div class="jd-section-employer"> <div class="jd-description-text"> <p><strong><span data-contrast="auto">Join Us in Shaping the Future of Clinical Research</span></strong><span data-ccp-props="{"335559738":200,"335559739":120}"> </span></p> <p><span data-contrast="auto">Adams Clinical is a leading clinical trial site network committed to accelerating the development of life-changing medicines. Our mission is simple: deliver uncompromising data quality, safety, and diverse enrollment to advance healthcare. Our vision is to set the gold standard for clinical trial excellence. We believe our people make the difference. Guided by our core values—</span><em><span data-contrast="auto">Scientific Rigor, Operational Excellence, Commitment to Sponsors and Participants, and Authentic Collaboration</span></em><span data-contrast="auto">—we create an environment where meaningful work drives meaningful change.</span><span data-ccp-props="{"335559739":160}"> </span></p> <p><span data-contrast="auto">At Adams Clinical, you’ll find:</span><span data-ccp-props="{"335559739":80}"> </span></p> <ul> <li data-leveltext="•" data-font="" data-listid="2" data-list-defn-props="{"335552541":1,"335559685":720,"335559991":360,"469769242":[8226],"469777803":"left","469777804":"•","469777815":"hybridMultilevel"}" data-aria-posinset="1" data-aria-level="1"><span data-contrast="auto">A culture of respect, transparency, and continuous improvement</span><span data-ccp-props="{"335559739":80}"> </span></li> </ul> <ul> <li data-leveltext="•" data-font="" data-listid="2" data-list-defn-props="{"335552541":1,"335559685":720,"335559991":360,"469769242":[8226],"469777803":"left","469777804":"•","469777815":"hybridMultilevel"}" data-aria-posinset="2" data-aria-level="1"><span data-contrast="auto">Opportunities for professional growth and learning</span><span data-ccp-props="{"335559739":80}"> </span></li> </ul> <ul> <li data-leveltext="•" data-font="" data-listid="2" data-list-defn-props="{"335552541":1,"335559685":720,"335559991":360,"469769242":[8226],"469777803":"left","469777804":"•","469777815":"hybridMultilevel"}" data-aria-posinset="3" data-aria-level="1"><span data-contrast="auto">A team dedicated to improving lives through innovation and integrity</span><span data-ccp-props="{"335559739":80}"> </span></li> </ul> <p><span data-contrast="auto">If you’re passionate about making an impact in clinical research and want to be part of a collaborative, mission-driven organization, we’d love to have you on our team.</span><span data-ccp-props="{"335559739":160}"> </span></p> <p><strong><span data-contrast="auto">Job Role</span></strong><span data-ccp-props="{"335559738":200,"335559739":120}"> </span></p> <p><span data-contrast="auto">Adams Clinical is seeking a detail-oriented and proactive eSource Architect to oversee the development, maintenance, and quality control of electronic source (eSource) documentation across our multi-site research network. This role plays a critical function in ensuring that source documentation is accurate, compliant, and operationally ready in alignment with ICH-GCP, FDA, and IRB requirements.</span><span data-ccp-props="{}"> </span></p> <p><span data-contrast="auto">The eSource Architect reports directly to the Associate Director of Quality Assurance and works closely with the Regulatory, Operations, and Finance teams to support both study start-up activities and the day-to-day management of source amendment requests. The successful candidate will balance efficiency and compliance, ensuring that eSource is finalized ahead of trial activation and that amendment requests are processed rapidly with precision.</span><span data-ccp-props="{}"> </span></p> <p><span data-contrast="auto">A central focus of this role is to optimize eSource design and workflows so that site clinical research staff can execute study protocols seamlessly, thereby reducing protocol deviations, improving protocol and regulatory compliance, and trial efficiency.</span><span data-ccp-props="{}"> </span></p> <p><strong><span data-contrast="auto">Key Responsibilities:</span></strong><span data-ccp-props="{"335559738":200,"335559739":120}"> </span></p> <ul> <li data-leveltext="" data-font="Symbol" data-listid="14" data-list-defn-props="{"335552541":1,"335559685":720,"335559991":360,"469769226":"Symbol","469769242":[8226],"469777803":"left","469777804":"","469777815":"multilevel"}" data-aria-posinset="1" data-aria-level="1"><span data-contrast="auto">Develop new source builds across all active and start-up studies within the site network, finalized in advance of site activation to ensure enrollment readiness.</span><span data-ccp-props="{"134233117":false,"134233118":false,"335559738":0,"335559739":0}"> </span></li> </ul> <ul> <li data-leveltext="" data-font="Symbol" data-listid="14" data-list-defn-props="{"335552541":1,"335559685":720,"335559991":360,"469769226":"Symbol","469769242":[8226],"469777803":"left","469777804":"","469777815":"multilevel"}" data-aria-posinset="2" data-aria-level="1"><span data-contrast="auto">Review and implement protocol amendment updates promptly, minimizing operational delays while safeguarding regulatory and protocol compliance.</span><span data-ccp-props="{"134233117":