adamsclinical · Philadelphia, Pennsylvania, United States · Philadelphia, Pennsylvania, United States
<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">The Clinical Research Regulatory Specialist serves as the regulatory owner for the </span><span data-contrast="auto">Philadelphia</span><span data-contrast="auto"> site, ensuring that every active study remains compliant and inspection ready from activation through closeout. This role combines hands on regulatory expertise with operational discipline, meticulous attention to detail, and close partnership with site operations to protect data quality and participant safety.</span><span data-ccp-props="{"335559739":120}"> </span></p> <p><span data-contrast="auto">The Clinical Research Regulatory Specialist is responsible for managing IRB approvals and amendments, maintaining staff credentialing and delegation, resolving sponsor and CRA action items, and sustaining continuous audit readiness. Reporting to the Central Regulatory Maintenance Manager, this position partners with site staff, PIs, sponsors, and CRAs, and collaborates with regulatory colleagues across our six-site network. Supported by twice weekly team check ins, monthly regulatory meetings, and centralized study start up support, the role is measured against specific goals tied to performance bonuses. This is an onsite position with potential for a couple of work from home days.</span><span data-ccp-props="{"335559739":120}"> </span></p> <p><strong><span data-contrast="auto">Key Responsibilities:</span></strong><span data-ccp-props="{"335559738":200,"335559739":120}"> </span></p> <p><strong><span data-contrast="none">IRB & Study Document Management</span></strong><span data-ccp-props="{"134245418":true,"335559738":140,"335559739":60}"> </span></p> <ul> <li data-leveltext="•" data-font="" data-listid="2" data-list-defn-props="{"335552541":1,"335559685":400,"335559991":240,"469769242":[8226],"469777803":"left","469777804":"•","469777815":"hybridMultilevel"}" data-aria-posinset="4" data-aria-level="1"><span data-contrast="auto">Distribute IRB approvals, amendments, and ICF updates, and verify that site staff are informed before study activities proceed.</span></li> <li data-leveltext="•" data-font="" data-listid="2" data-list-defn-props="{"335552541":1,"335559685":400,"335559991":240,"469769242":[8226],"469777803":"left","469777804":"•","469777815":"hybridMultilevel"}" data-aria-posinset="4" data-aria-level="1">Submit continuing reviews, protocol deviations, and other required reports to the IRB within established timelines.</li> <li data-leveltext="•" data-font="" data-listid="2" data-list-defn-props="{