
51 - 200 employees
Founded 2006
🧬 Biotechnology
💊 Pharmaceuticals
🔬 Science
Biotechnology • Pharmaceuticals • Science
Precision BioSciences, Inc. is a clinical-stage biotechnology company developing in vivo and ex vivo genome editing and cell therapy medicines using its proprietary ARCUS nuclease technology. The company focuses on potentially curative treatments for hard-to-treat and rare genetic diseases (including chronic hepatitis B, Duchenne muscular dystrophy, and mitochondrial disorders) and allogeneic CAR T cell therapies for oncology. Precision BioSciences advances programs through preclinical and clinical trials, maintains collaborations and licensing agreements with biopharma partners, and pursues patent protection for its ARCUS platform and specific therapeutic candidates.
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51 - 200 employees
Founded 2006
🧬 Biotechnology
💊 Pharmaceuticals
🔬 Science
Biotechnology • Pharmaceuticals • Science
Precision BioSciences, Inc. is a clinical-stage biotechnology company developing in vivo and ex vivo genome editing and cell therapy medicines using its proprietary ARCUS nuclease technology. The company focuses on potentially curative treatments for hard-to-treat and rare genetic diseases (including chronic hepatitis B, Duchenne muscular dystrophy, and mitochondrial disorders) and allogeneic CAR T cell therapies for oncology. Precision BioSciences advances programs through preclinical and clinical trials, maintains collaborations and licensing agreements with biopharma partners, and pursues patent protection for its ARCUS platform and specific therapeutic candidates.
• Serve as a primary scientific interface site-level contact for investigators and site medical staff within responsible geography • liaising with Clinical Operations, the CRO and the Medical Monitor who maintain primary contacts for site operations • Lead site-level training on protocol procedures and staff support • Understand the patient journey in the trial at the clinical site and work with staff to facilitate improvements • Meet with all staff who will be assessing patients to ensure consistency with assessments • Educate staff about PBGENE-DMD; Train fellows & residents that cycle through the clinical site • Provide frequent updates to Clinical team to support ongoing recruitment • Partner with Clinical Development, Clinical Operations, Program Management and Corporate Communications team to support compliant scientific education for advocacy organizations and patient communities • Support investigator engagement and relationship management alongside Clinical Development leadership
• Bachelor's degree (or equivalent) and 7+ years of total experience in clinical research, medical affairs, patient advocacy, or clinical practice within biotech, pharma, and/or clinical trial site(s), or equivalent combination of education and experience • Direct experience in pediatric rare disease or neuromuscular therapeutic areas • Demonstrated experience managing clinical trial site relationships • Track record of engagement with patient advocacy organizations • Strong scientific communication skills; ability to translate complex data for diverse audiences • Willingness to travel up to 60-70% at peak
• Health insurance • 401(k) matching • Flexible work hours • Paid time off • Remote work options
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