Regulatory Affairs Associate (Contract)

Attention recruitment agencies: All agency inquiries are vetted through 4DMT’s internal Talent Acquisition team. No unsolicited resumes will be accepted. The 4DMT Talent Acquisition team must expressly engage agencies on any requisition. Agencies contacting hiring managers directly will not be tolerated, and doing so may impact your ability to work with 4DMT in the future. 4DMT is a leading late-stage biotechnology company advancing durable and disease-targeted therapeutics with potential to transform treatment paradigms and provide unprecedented benefits to patients. The Company’s lead product candidate 4D-150 is designed to be a backbone therapy forming the foundation of treatment of blinding retinal vascular diseases by providing multi-year sustained delivery of anti-VEGF (aflibercept and anti-VEGF-C) with a single, safe, intravitreal injection, which substantially reduces the treatment burden associated with current bolus injections. The Company’s lead indication for 4D-150 is wet age-related macular degeneration, which is currently in Phase 3 development, and second indication is diabetic macular edema. The Company’s second product candidate is 4D-710, which is the first known genetic medicine to demonstrate successful delivery and expression of the CFTR transgene in the lungs of people with cystic fibrosis after aerosol delivery GENERAL SUMMARY The Regulatory Affairs Associate at 4D Molecular Therapeutics, Inc. (4DMT) will be supporting the Regulatory Project Team (RPT) to ensure the successful progress of 4DMT’s product pipeline toward regulatory approval and commercialization. The role will work within the RPT and with both internal and external stakeholders to ensure timely review and approval of various regulatory submissions. This role can be remote or hybrid. Strong preference is given to SF Bay Area/West Coast candidates. MAJOR DUTIES & RESPONSIBILITIES: • Support US and global submission preparation by drafting and formatting relevant documents, coordinating cross-functional (e.g., CMC, nonclinical, and clinical) deliverables, and scheduling submissions. • Ensure regulatory submissions' quality, completeness, accuracy, and compliance. • Support Health Authority interactions by preparing relevant documents and plans. • Attend cross-functional and departmental meetings. • Assist in the maintenance of regulatory dashboards, plans, timelines, and support tools. • Assist with regulatory intelligence and strategic planning. • Builds and maintains current knowledge of applicable regulatory requirements and performs assigned activities in accordance with company procedures and applicable regulations. • Other duties as assigned, nothing in this job description restricts management’s right to assign or reassign duties and responsibilities to this job at any time. QUALIFICATIONS:  Education:  • Minimum Bachelors degree in a relevant field. • Advanced certificate or degree a plus. Experience:  • 1+ years of drug development experience in regulatory, clinical research/operations, clinical quality assurance, and/or medical writing. • Experience with gene therapy/biologics or ophthalmology therapeutic area a plus. Other Qualifications/Skills:  • Basic to intermediate knowledge of 21 CFR, ICH, and GCP guidelines. • Basic to intermediate knowledge of CTD structure, format, and submission requirements. • Ability to work in a team-based environment, cooperatively and supportive of multiple viewpoints and approaches. • Flexibility and ability to prioritize and manage multiple tasks and projects simultaneously. • Proficiency with Microsoft Word, Outlook, SharePoint, and Adobe Acrobat. • Excellent oral and written communication skills. • Strong attention to detail and organizational skills. Travel: Physical R