4dmoleculartherapeutics Executive Medical Director at 4dmoleculartherapeutics providing strategic Quality Assurance leadership for global clinical trials. Responsible for ensuring compliance with GCP and advancing clinical quality systems.
Responsibilities
Serve as clinical lead for Phase 1 retina clinical trials including study design and protocol development
Maintain accountability for study execution, data interpretation, and clinical readouts
Serve as medical monitor ensuring subject safety and data integrity
Lead cross-functional study teams to ensure timely trial delivery
Provide clinical leadership to multidisciplinary study execution teams
Lead development and implementation of biomarker strategies
Collaborate with research and translational teams to integrate biomarkers into trials
Qualification
Bachelor's degree in a life scienceExperience hostingOther Qualifications/SkillsExecutive-level communication skillsStrong leadership
Required
Bachelor's degree in a life science, nursing, pharmacy, or related field; advanced degree (MS, PharmD, PhD) preferred.
12+ years of experience or advanced degree with 10+ years of experience within a regulated environment such as Regulatory, Quality, Pharmacovigilance or Clinical Development / Operations within the Biotech or similar
Proven experience leading Clinical quality strategy, quality governance, and senior-level quality oversight of global clinical trials and associated vendors
Minimum of 7 years of significant experience in clinical quality assurance, including experience leading, performing, and/or providing senior oversight of GCP audits and global clinical trials.
Experience hosting, leading, and supporting health authority inspections, including inspection readiness preparation, front-room/back-room support, response coordination, and follow-up commitment management
Extensive practical experience and understanding of clinical quality assurance applied throughout the clinical development life-cycle
Demonstrated ability to influence senior cross-functional stakeholders, lead complex clinical quality initiatives, and provide mentorship or functional leadership within Clinical QA
Other Qualifications/Skills:
Expert understanding of GCP requirements for investigational products and the ability to interpret and apply requirements strategically across clinical programs
Executive-level communication skills, both oral and written, with ability to present quality risks, recommendations, and inspection-readiness status to senior stakeholders
Strong leadership, influencing, and interpersonal skills, with a collaborative approach to driving alignment across Clinical, Quality, Regulatory, and external vendor stakeholders
Demonstrated ability to operate independently in a fast-paced small company environment, prioritize complex workstreams, make risk-based decisions with minimal direction, and adjust quickly to changing business priorities