Hiring: Precision Oncology Clinical Trial Coordinator Company: Lantern Pharma Inc. (Nasdaq: LTRN) Location: Plano, TX Job Posted Time: 2026-09-15 13:00:15 Employment Type: Full-time / Hybrid Target Skills & Keywords : GCP, Rails, Regulatory Compliance About the job Experience: •5+ years in clinical research operations at a sponsor, CRO, or high-volume oncology site. We care more about ownership of studies than a perfect title match. Required Skills: •Lantern Pharma is an AI-driven precision oncology company developing targeted therapies with our RADR® platform. We run lean: the person who owns day-to-day trial operations is the connective tissue between sites, vendors, monitors, and clinical leadership — not a back-office processor. •Help execute biomarker-driven oncology studies in indications such as triple-negative breast cancer, recurrent GBM / CNS tumors, and other DNA-damage-repair–selected solid tumors. In a small public biotech, your work shows up in enrollment, clean data, regulatory compliance, and how fast we can amend a protocol and keep sites moving. •Primary operational contact for investigators, coordinators, nurses, clinical monitors and vendors. Build relationships that improve screening, enrollment, and compliance. Track recruitment and outcomes in real time and flag bottlenecks early. Partner with relevant patient advocacy groups on recruitment strategy. •Support start-up and close-out with monitors; keep SOPs and the study project plan current. First-line review of monitoring reports; drive CAPAs at sites and vendors to closure; log and trend study deviations; lead study-specific deviation meetings. Join data reviews (coding, deviations, safety) so queries do not stall trial procedures. •File final study documents promptly in QDMS and keep the forward regulatory documents for filing in the eTMF.  Help review and edit IRB / ethics submissions and amendments. Track IP, lab kits, and supplies. Compile clinical inquiries into FAQs and help the Medical Monitor get clear guidance to sites in urgent situations. •Day-to-day coordination of contracted monitors and similar study-support roles; escalate risk early. •Success in the first 90 days •You know every active site, the coordinator, and where each site sits on screening and enrollment. Qualifications: •Bachelor’s in life sciences, nursing, public health, or a related field. •3–5+ years in clinical research operations at a sponsor, CRO, or high-volume oncology site. We care more about ownership of studies than a perfect title match. •Solid functional working knowledge of FDA regulations and ICH-GCP, including familiarity with E6(R3) risk-based / quality-by-design direction. •Hands-on eDC and eTMF experience; comfort with trackers, query reports, and version-controlled files. •Calm, precise work with investigators and site staff; strong written communication and an audit trail others can follow. •Able to work independently in a small team and move between start-up, enrollment, and close-out in the same week. •Live in the Dallas / Plano area and be in the Plano office 2–3 days per week. •Preferred — none of these are blockers •RN, BSN, MPH, or similar credential; ACRP / SOCRA (CCRC or CCRP) or willingness to obtain. •Oncology or biomarker-selected protocol experience; multi-country or academic-center sites. Compensation: •Competitive pay plus stock option grants; health, dental, and vision; 401(k) with match Interested candidates, please apply directly through the job posting on company's career page or try via AI auto apply on this platform. Don't miss this opportunity to join a forward-thinking team!