Regulatory Affairs Coordinator

Description Position Title: Regulatory Operations Coordinator / Manager Reporting to: Vice President, ASO Discovery and Development Hours: Full-Time Location: Hybrid Compensation: $85,000-$110,000 (may vary based on relevant skills, experience, and qualifications) n-Lorem Foundation Though n-Lorem is pioneering a novel non-profit model, to provide personalized experimental ASO treatments for free, for life to patients with the rarest of mutations (nano-rare), we are functionally a biotechnology company. We have a large and growing portfolio of ASO medicine discovery programs, ASO medicines in development and multiple clinical programs. With a seasoned leadership team and strategic partnerships, the n-Lorem Foundation provides the framework, funds and access for nano-rare patients who are amenable to our technology to receive personalized ASO medicines for free, for life. We hope that you will consider joining us as we strive to change the world, one nano-rare patient at a time. If you are a professional with strong Regulatory Operations experience and would like to join a cohesive, experienced team committed to the belief that we can change the world one patient, one family at a time, we may have a position for you. Job Overview The Regulatory Operations Coordinator / Manager will be responsible for the operational aspects of n-Lorem's regulatory activities, in the U.S., while also supporting the preclinical and clinical development teams in the development, authoring, editing, reviewing and/or processing of various documents directly or indirectly related to regulatory submissions. We are seeking an experienced individual with strong attention to detail who is quick and eager to learn, goal-oriented, and self-motivated. The successful candidate will work closely with the preclinical and clinical development teams to implement efficiencies in regulatory operations across the n-Lorem portfolio of ASOs. The ability to thrive in a fast-paced biotech-like environment is essential. Job Duties Collaborate with cross functional teams to develop timelines for submissions to regulatory authorities. Support the authoring of high-quality regulatory communications, including regulatory meeting requests, briefing packages, responses to regulatory health authority requests, and IND components. Track upcoming regulatory milestones, including initial submissions, hold and non-hold responses and annual reports. Track, maintain and file all regulatory documentation. Gather input from key stakeholders to efficiently respond to inquiries from regulatory agencies in a timely manner. Prepare IND annual reports. Collaborate with the Clinical Development team to coordinate site IRB review and approval. Prepare new clinicaltrials.gov listings and provide annual updates. As needed, support cross-functional teams in n-Lorem's global expansion efforts. Provide crisp review of data or reports that will be incorporated into regulatory submissions to assure scientific rigor, accuracy, consistency, and clarity of presentation. Develop, maintain, and improve templates for various documents, including nonclinical or clinical protocols, cover letters, pharmacy manuals, IND sections, or others. Prepare and revise internal regulatory procedures for continuous improvement. Perform other duties as assigned to contribute to the development of the infrastructure needed to support an ever-growing portfolio of programs at various stages. May require up to 10% travel. Requirements U.S. work authorization. BSc or MS degree in a scientific discipline required. Minimum of 3 years of experience working in the pharmaceutical, biotechnology. or clinical research industry. Working knowledge of FDA regulations and guidance relevant to clinical-stage drug development. Strong attention to detail and the ability to maintain accuracy in a fast-paced, evolving environment. Demonstrated ability to collaborate effectively across cross-functional teams. Demonstrated organizational and project management skills, with the ability to coordinate multiple regulatory activities, manage competing priorities, and consistently meet timelines. Self-motivated, proactive, and hands-on, with a strong sense of ownership and accountability. #J-18808-Ljbffr