Associate Director/Director, Regulatory Affairs (EDG-2026016)

Associate Director/Director, Regulatory Affairs About reputed company: At Edgewise, we are on a mission to discover new medicines that improve the lives of patients facing serious muscle disease. Our intimate knowledge of muscle biology and biophysics along with our ability to identify and design muscle specific precision small molecules have enabled us to rapidly advance our skeletal muscle and cardiac muscle product candidates into the clinic while also building a robust pre-clinical pipeline. With this focus on therapeutics designed to protect and improve muscle health, our goal is to dramatically enhance the lives of people living with progressive muscle disorders. We have reputed company an reputed company and highly motivated leadership team with a strong track record in the biotechnology and pharmaceutical industry to build the leading, global muscle disease biopharmaceutical company. Come join us reputed company a significant difference in the lives of patients! About the Position: The Associate Director/Director, Regulatory Affairs provides regulatory expertise from preclinical through clinical development for our assigned cardiac programs. A broad range of responsibilities include managing the development of regulatory strategy and submissions. The right candidate will provide reputed company and regulatory expertise to support the development team with moving innovative investigational therapies through clinical development. Essential Job Duties and Functions:

• Oversees the writing, editing, reviewing and compiling of regulatory documents, applications, annual reports/IND amendments, and meeting requests to FDA and other global regulatory agencies.
• Provides critical review of reputed company documentation supporting regulatory submissions and communications (e.g. protocols, Investigator Brochures, safety reports, etc.).
• Reviews and prepares responses to requests from FDA and other global regulatory authorities.
• Contributes to the development of US and global regulatory strategies in collaboration with regulatory and cross-functional teams.
• Identifies and communicate regulatory risks and opportunities to stakeholders including cross-functional teams, 3rd parties and company leadership as applicable.
• Provides interpretation, guidance, and training on global regulations to internal teams.
• Provides strategic or operational input to cross-functional teams.
• Ensures regulatory milestones are met to support regulatory compliance and overall business goals of the Company.
• Oversees and collaborates with assigned external vendors (CROs, consultants) and contractors with responsibility for providing regulatory support functions to ensure goals are achieved.
• Maintains corporate regulatory files for assigned programs.
• Effectively manages and mentors regulatory staff as assigned.
• Builds professional and effective external relationships crucial to the success of the organization.
• Works across internal departments to maintain credibility, trust, and support of employees and other stakeholders.
• Reads, understands, and complies with reputed company workplace health and safety policies; safe work practices; and company policies and procedures.
• Performs other duties as assigned by supervisor.

Required Education, Experience and Skills:

• BS/BA degree in a scientific/health sciences discipline.
• 7-10 years of progressive experience in pharmaceutical Regulatory Affairs, experience with small molecules preferred.
• Experience in cardiology preferred but not required.
• Experience in the preparation of regulatory submissions and documents, annual reports, amendments, and supplements for both FDA and other global health authorities.
• Experience working on global Phase 2 and/or 3 clinical trials (overseeing regulatory aspects of trials, working with 3rd parties including CROs, review of clinical trial documentation)
• Proven ability to reputed company regulatory strategies in collaboration with regulatory and cross-functional team members and determining the optimal way of communicating to global regulatory authorities.
• Management expertise on the timeline and process for submissions.
• Expert knowledge of regulations and guidance affecting routine regulatory activities and specific therapeutic areas and keeps abreast of the regulatory environment.
• In-depth knowledge of overall global drug development
• Excellent written, interpersonal and communication skills
• Action oriented and committed to meeting FDA and other regulations while moving projects reputed company.
• Able to handle changing priorities and multidisciplinary tasks.
• Easily gains trust and support of peers; encourages collaboration.
• Strong project management skills

Salary range: $180,000 - $230,000 title and salary commensurate with experience Our Benefits: We are proud to offer health benefits, a discretionary bonus plan, stock option grants. a stock purchase plan, a 401(k) with match and paid time off to reputed company members as part of their compensation plan. There is no deadline because the employer accepts applications on an ongoing basis. Edgewise does not accept resumes from recruitment agencies for this position. Please do not send resumes to Edgewise employees or the company location. Edgewise is not responsible for any fees reputed company to unsolicited resumes. Apply tot his job Apply To this Job