Director Of Regulatory Affairs

Hemab seeks a Director, Regulatory Affairs who will be responsible for developing and executing innovative global regulatory strategies for the global development of candidates for the treatment of rare, hematological disorders. This position will define, develop, and lead execution of strategies to maximize global regulatory success and achieve program objectives for complex development projects in the rare disease space. The Director Regulatory Affairs will be response for keeping abreast of new developments in regulatory science and maintaining oversight on the evolving regulatory landscape and advancing innovations. In addition, the Director Regulatory affairs must understand and interpret scientific data as it relates to regulatory requirements and strategy for assigned projects and provides knowledge and expertise to guide team in established and building appropriate regulatory strategy.

This role is expected to be a leader, contributing to cross-functional initiatives and influencing the field, as applicable. You may represent Hemab in industry/regulatory forums to lead regulatory innovation. This role is ideally suited to a candidate who is self-motivated and excited by an opportunity to rise to frequent and diverse challenges.

Duties/Responsibilities:

• Oversee vendor responsibility for regulatory activities and submissions related to projects within scope.
• Participates with influence in or leads departmental and cross-functional taskforces and initiatives.
• Effectively communicates through presentations and written communications regulatory strategies and project developments to project teams, colleagues, line management, and key stakeholders for alignment and to ensure awareness of issues that may impact regulatory success. Communications demonstrate sound judgement and are provided in a professional and timely manner.
• The Sr Director/Director will be accountable for all Regulatory Agency submissions and approvals of project(s) of responsibility, overseeing outsourced vendors and/or Hemab internal team members.
• Will be responsible for complex and potentially multiple projects within the Rare Disease space. Responsible for development of regulatory strategies related to development and licensure of biologic development products. Represents Regulatory Affairs at project team meetings.
• Direct point of contact with health authorities, leads and manages Regulatory Agency meetings, in cooperation with outsourced vendors.
• Partner with global market access colleagues to lead interactions with joint regulatory/health agency/HTA bodies on product specific value evidence topics, as applicable.
• Monitor and anticipate trends that impact both the regulatory and access environments to strengthen product development plan(s) and adopt regulatory strategies in a timely manner.
• Collaborate across technical functions to create innovative regulatory strategies for projects and pragmatic solutions to deliver on the proposed strategy with the project teams.
• Responsible for proactively anticipating regulatory risks and for developing mitigation strategies in alignment with team and management; understands relative strengths, weakness, and probabilities of technical success for the mitigation strategies proposed.

Qualifications and experience:

• [Sr Director] 12+ years of pharmaceutical industry experience inclusive of 10 years of regulatory experience or a combination of 8+ years of regulatory and related experience.
• [Director] 8+ years of pharmaceutical industry experience. This is inclusive of 6 years of regulatory experience or a combination of 5+ years regulatory and/or related experience. Experience in rare diseases, especially rare hematological disorders, preferred.
• Bachelors degree in a scientific subject area coupled with sufficient industry experience. Advanced degree (e.g. MSc, PhD, PharmD, MD) preferred.

Skills and abilities:

• Ability to advise on applicable regulations and guidance documents, including providing interpretation of these governing documents by regulators as experience is gained in practice.
• Demonstrated ability to work well within global teams and success leading cross-functional regulatory work products.
• Understands and interprets scientific data as it relates to regulatory requirements and strategy for assigned projects and provides knowledge and expertise to guide team in established and building appropriate regulatory strategy.
• Strong oral and written communications, managing and adhering to timelines, negotiation skills, integrity, and adaptability.
• Demonstrates acceptable skills with increasing independence in the area of regulatory strategy such as understanding broad concepts within regulatory affairs and implications across the organization and globally; proactively identifies regulatory issues; offers creative solutions and strategies, including risk mitigation strategies.
• Understands and works effectively with team members and consultants to develop the regulatory framework for the clinical development of small molecules and biologic products leading to global marketing authorizations.
• Keeps abreast of new developments and therapeutic innovations, including regulatory requirements related to gene therapy and associated science.

Physical Demands:

• Ability to remain seated for long periods of time while working on computer or referring to documents.
• Must have manual dexterity to operate computer keyboard and standard office equipment.
• Travel may be required (up to 25% of the time).
• Positions: Standing, walking, sitting, stooping.

Hemab Therapeutics is an Equal Opportunity and Affirmative Action employer committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.

As a healthcare company, Hemab has an important responsibility to protect individual and public health. All roles require individuals to be fully vaccinated against COVID-19 as part of your job responsibilities.