Senior Director, Global Regulatory Lead
Posted on May 14, 2019 by Jazz Pharma
Jazz Pharmaceuticals is an international biopharmaceutical company focused on improving patients' lives by identifying, developing and commercializing meaningful products that address unmet medical needs. We are continuing to expand our commercial product portfolio and our research and development pipeline in therapeutic areas that can leverage our unique expertise.
Our therapeutic areas of focus include sleep and hematology/oncology - areas in which we have a deep understanding of the patient journey and a suite of products and product candidates to address critical needs.
We are looking for the best and brightest talent to join our team. If you're looking to be a part of a company with an unwavering commitment to improving patients' lives and being a great place to work, we hope you'll explore our career openings and get to know Jazz Pharmaceuticals.Responsibilities:
The Global Regulatory Lead (GRL) will be responsible for developing and delivering innovative, breakthrough global regulatory strategies for a product in assigned therapeutic area. The GRL will be responsible for regulatory aspects related to product development and approval, in alignment with the global business strategy and in partnership with the functional subject matter experts within Global Regulatory Affairs.
- Member of the Global Molecule Team:
- Represents Global Regulatory Affairs (GRA) as a member of the cross functional matrix Global Molecule Team (GMT). Responsible for ensuring collaboration with key internal stakeholders of the GMT and the Development Core Team (DCT) to ensure successful planning and execution of the global regulatory strategy for assigned program(s).
- Accountable for the development and maintenance of a global regulatory strategy plan. In conjunction with GRT ensure that relevant input is vetted and included in the regulatory strategy in order to deliver on the Target Product Profile (TPP), regional specific needs, regulatory environment, regulatory risks and mitigations, and global submission strategies.
- Identify and assess regulatory risks associated with product development and recommend strategies to mitigate risks.
- Ensure appropriate representation of regulatory affairs on key internal program/project teams. Ensure strategic regulatory input is provided to key development activities and documents, including clinical protocols, clinical and nonclinical reports and summary documents, statistical analysis plans, etc. Leverage GRT as appropriate to ensure appropriate input is provided throughout the development process.
- Lead Global Regulatory team for assigned molecule(s):
- Facilitate exceptional regulatory team performance by leading regulatory team meetings (GRT) and collaborating with regional regulatory strategists, regulatory sub-function
- representatives, and engaging GRA leadership for a strong and broad regulatory strategy and execution of regulatory deliverables
- Ensure a well-functioning GRT and nurture an environment where all GRA team members and functions have a voice
- Pro-actively support the regional strategy leads on the establishment and maintenance of high quality working relationships with regulatory agencies as appropriate for assigned therapeutic areas and products. Includes effective planning and presentation of key meetings with Health Authorities to ensure full discussion of issues and opportunities.
- Work with the GRT for preparation of clear and effective Regulatory submissions e.g., INDs, NDAs/BLAs, CTAs, MAAs, supplements and other relevant regulatory filings.
- Depending on the program assignment, the GRL may also serve as the Regional Strategy Lead
- Responsible for ensuring requirements to maintain marketing applications and regulatory approvals are achieved within specified timelines. Oversee and work with regional leads (EU/RoW and US) to ensure consistent approach within molecule and maximize regional efficiencies.
- Accountable to GRA and the organization:
- Communicate project updates and risks to Regulatory Leadership and other stakeholders across the organization. Track regulatory commitments and ensure timely execution of regulatory deliverables
- Monitor and analyze appropriate regulatory agency activities and industry precedence in areas of interest to the company, and assess impact on programs
- Support Global Regulatory Leadership team in developing and adhering to functional area operational budgets for all programs
- Mentor guide direct reports in carrying out responsibilities. Responsible for coordinating activities and career development of direct reports
- Other duties as assigned
Required Knowledge, Skills, and Abilities
- Minimum 10 years of experience in Global Regulatory Affairs, including a minimum of 8 years' experience in drug development and registration activities; prior experience in relevant therapeutic area strongly preferred
- Experience interfacing with regulatory agencies and proven skill at developing and implementing successful global regulatory strategies
- Thorough knowledge and understanding of regulatory requirements for pharmaceutical/biological product development and approval in more than one key region (ie. US, EU, Japan)
- Track records of issue resolutions with main regulatory authorities; demonstrated ability to break down complex, scientific content into logical components.
- Experience with developing and documenting regulatory strategies in coordination with clinical plans and marketing objectives.
- Experience with communicating the regulatory strategy, issues, and risks in written and verbal format to regulatory senior leadership team and other governing bodies.
- Ability to broadly represent department functions on project team in a matrix organization. Demonstrated ability to coordinate global activities
- Experience in leading and managing matrix teams (minimum 3-5 years), setting clear direction, holding people accountable and fostering a collaborative team environment
- Prior line management experience in a global organization
- Excellent verbal and written communication skills and collaborative interpersonal skills
- Ability to broadly represent department functions on project team in a matrix organization and demonstrated ability to coordinate global activities
Required/Preferred Education and Licenses
- Bachelor's degree is minimum required, Master's degree or advanced degree in a scientific discipline is preferred
Description of Physical Demands
- Occasional mobility within office environment.
- Routinely sitting for extended periods of time.
- Constantly operating a computer, printer, telephone and other similar office machinery.
Description of Work Environment
- Work indoors in normal office environment with little exposure to excessive noise, dust, fumes, vibrations and temperature changes.
- Frequent computer use at workstation.
- May move from one work location to another occasionally.
- Responsibilities may require a work schedule that may include working outside of "normal" work hours, in order to meet business demands.
- Occasional public contact requiring appropriate business apparel.
Jazz Pharmaceuticals is an equal opportunity/affirmative action employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any characteristic protected by law.