Position : Senior Director / Vice President, Clinical Development

Before applying for this role, please read the following information about this opportunity found below. Salary Range : 200-250K Location : Boston, MA Metro Area We are looking for a senior clinical developer to take on strategic and medical leadership in a late-stage program, in addition to larger research and development pipeline responsibilities. This role will handle clinical research development, implementation, and supervise pre-clinical and clinical research activities to pursue product development goals. This role will involve working closely with operations and internal teams to ensure regulatory compliance as well as scientific and industry standards. The right candidate will have robust experience in drug development with documented success in late-stage clinical trials. Key Responsibilities Define and drive target product profiles and clinical development strategies for key programs Lead cross-functional teams in planning and executing preclinical and clinical activities across the development pipeline Act as clinical lead for new opportunity assessments and business development efforts Oversee the creation, review, and approval of clinical trial documents, including protocols, synopses, Investigator Brochures, and study reports Manage all aspects of clinical trials—from planning and conduct to data analysis and reporting Approve safety management plans, medical monitoring, and protocol deviation handling Analyze and interpret clinical data, contribute to statistical planning, and support publication strategies Lead or support literature reviews, meta-analyses, and scientific writing efforts Support regulatory submissions and respond to health authority inquiries Collaborate closely with internal and external partners to ensure effective study execution and resolve issues efficiently Ensure adherence to clinical trial registry and disclosure requirements Publications & External Engagement Lead development and review of abstracts, posters, and manuscripts Partner with clinical operations and medical affairs on investigator-initiated studies and research collaborations Qualifications Bachelor’s degree in a scientific field required; advanced degree (MD, PhD, PharmD, or equivalent) strongly preferred 15+ years of hands-on experience in clinical research and drug development, covering early- to late-stage trials and regulatory interactions Strong background in trial design, operations, data management, and scientific communications Proven success in leading late-stage clinical programs and cross-functional R&D initiatives Deep understanding of regulatory requirements and clinical compliance To apply please send your resume to aaron.bacon@lumicity.io

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