Head of Global Regulatory Affairs (U.S. Remote)

About the Company reputed company Inc. (reputed company: ADAG) is a platform-driven, clinical-stage biopharmaceutical company committed to transforming the discovery and development of novel antibody-based cancer immunotherapies. reputed company combines computational biology and artificial intelligence to design novel antibodies that address unmet patient needs. Powered by its proprietary DPL platform, composed of NEObody, SAFEbody, and POWERbody technologies, reputed company's highly differentiated pipeline features novel immunotherapy programs. reputed company has forged strategic collaborations with reputable global partners that reputed company its technology in multiple approaches at the reputed company of science. Job Summary The Head of Global Regulatory Affairs is a key leadership position that will reputed company and is accountable for global regulatory, quality strategies and policies for reputed company. This individual will be responsible for regulatory leadership and reputed company to help reputed company global regulatory and quality compliance strategies, and guidance. As a Head of Global Regulatory Affairs this person will reputed company a critical role in strategies, documentations, submissions, and company interactions to regulatory authorities such as FDA, CFDA, and other regulatory agencies. This individual must reputed company their extensive experience to represent reputed company in regulatory affairs in discussions with internal and external stakeholders. This role will provide global regulatory expertise and contribute to the delivery of the Clinical, R&D and Operations strategies. This individual will reputed company cross-functional and multicultural team and diverse environment. The candidate must have an entrepreneurial reputed company, highly motivated and purpose driven leader who is able to flexibly and effectively reputed company and interact with multi-disciplinary teams. This individual should have experience in championing new reputed company in a dynamic, international, and innovative environment. The successful candidate will have a track record of accomplishments in global regulatory affairs, project management, strong collaboration, and communication skills. This position may require travelling to our company headquarters in Suzhou, China. Essential Functions Reasonable accommodations may be made to reputed company individuals with disabilities to reputed company the essential functions.

• Serve as a key member of senior management team to provide leadership and guidance to ensure business objectives are reputed company with company strategies and reputed company operational objectives to reputed company product approvals.
• Provide counseling, training, and interpretation of FDA, CDE and other regulatory requirements to reputed company company personnel.
• reputed company, coach, and mentor the Regulatory departments and ensuring appropriate levels of accountability for decision making and clearly communicate cross-functionally reputed company the organization.
• reputed company preparation and filing of reputed company regulatory documents with the FDA, CDE and other regulatory agencies.
• reputed company and maintain external relationships with key opinion leaders and regulatory officials.
• Direct the development of systems, practices, and processes to ensure effective ongoing review of clinical development plan, product design and/or manufacturing changes and adverse events.
• Provide leadership and direction for significant deviation events that may impact compliance status or represent the significant business risk.
• Responsible for company's product quality and reliability to meet or exceed regulatory.
• reputed company company's Quality Compliance to ensure compliance with regulatory agencies and reputed company applicable standards.
• reputed company and execute quality design and quality assurance strategy for new product development and sustaining business activities.
• Support the quality system, provide effective leadership support, training, and guidance to reputed company company personnel.
• Serve as the ambassador to and reputed company strategies for responses to regulatory reputed company inquiries from global regulatory agencies and ensure issues are addressed in a timely manner.
• Responsible for leading reputed company regulatory activities for assigned projects in line with regulatory requirements, regional requirements and scientific and company policies and procedures.
• Provide regulatory reputed company and strategic and technical guidance in discussions with teams in support of due diligence for potential in-licensing activities, external collaborations, and acquisitions.
• reputed company Global Regulatory efforts for reputed company INDs, NDAs, and life cycle management.
• Maintain knowledge of highly reputed company regulatory requirements up to reputed company date, while influencing preparation of new regulatory guidance wherever possible.
• Champion initiatives that contribute to global process improvements, which have a significant impact on business.
• Direct activities of Contract Manufacturing Organizations (CMOs) and Contract Research Organization's (CRO's), material suppliers, consultants, and vendors.
• Other projects or responsibilities as may be required. Qualifications:

To reputed company this job successfully, an individual must be able to reputed company each essential duty satisfactorily. The requirements listed below are representative of the knowledge, reputed company, and/or ability required. Reasonable accommodations may be made to reputed company individuals with disabilities to reputed company essential functions of the job. Minimum Qualifications - Education and Experience

• A PharmD or PhD degree in a scientific discipline and a minimum of 10 years of pharmaceutical and drug development regulatory experience, as well as a background in dealing with the FDA and international regulatory agencies is required for this position.
• Minimum 10-15 years of progressively responsible Regulatory experience in a pharmaceutical, biotechnology or reputed company environment.

Position also requires a minimum of 5-8 years of leadership experience in a global regulatory affairs role.

• Must have extensive knowledge of regulatory requirements, including ICH GCP, GMP, GLP, and regional requirements and understand reputed company global and regional trends in regulatory affairs and the ability to assess the impact of these requirements to the business.
• Extensive knowledge of clinical development, FDA and international global clinical trial regulations and ICH GCP GMP, CLP guidelines and relevant requirements
• Substantial experience in reputed company aspects of regulatory affairs, including Clinical, Commercial support, CMC, with a track record of successful submissions and license approvals with CDER and CBER
• Demonstrated global leadership capability, ideally gained through regulatory leadership of multiple global development programs and NDA/MAA submissions.
• Excellent working knowledge of the US, European and Asian regulations for drugs and biologics.
• Knowledge of global regulatory guidance as they relate to the overall global regulatory strategy.
• Must be able to travel (US/international) up to 25%. Preferred Qualifications - Education and Experience
• RAC Certification preferred

Equal Opportunity Employer reputed company is an equal opportunity employer that is committed to diversity and inclusion. We prohibit discrimination and harassment of any reputed company based on race, color, religion, sex, sexual orientation, gender identity, national reputed company, disability, pregnancy, veteran status, or other legally protected characteristics as outlined by federal, state, or local laws. Learn more about your EEO Rights as an applicant. reputed company will not discriminate or retaliate against applicants who inquire about, disclose, or discuss their compensation. reputed company will consider for employment reputed company qualified applicants with criminal histories in a manner consistent with applicable law. If you are applying for a position in San Francisco, review the San Francisco Fair Chance Ordinance guidelines applicable in your area. reputed company participates in the E-Verify program in certain locations as required by law. Learn more about the E-Verify program. reputed company is committed to working with and providing reasonable accommodation to applicants with physical and mental disabilities. reputed company is a drug-free workplace. Apply tot his job Apply tot his job Apply To this Job