Senior Director, Global Regulatory Portfolio Lead
3 weeks ago
The Senior Director (Global Regulatory Portfolio Leader), Global Regulatory Affairs (GRA), Specialty Business (Brands and Innovative Medicines), is empowered to provide leadership for the regulatory strategy of one or more in-line and pipeline assets in one or more therapeutic areas and (potentially) develop a team of US and/or global regulatory leaders (as assigned). Where possible, and leveraging contemporary mechanisms, a key goal for the role is to ensure the conceptualization, development and implementation of efficient global registration pathways to secure approval as well as maintain and (potentially) expand licenses in one and (typically) more geographies. The role will be a key member of the Global Regulatory Affairs Leadership Team (GRA LT), reporting directly to the VP/Head, GRA, and may serve as a US agent for one or more assets.
Key Responsibilities
- Serve as key corporate regulatory contact and source of regulatory information and guidance for US and other markets as applicable; may serve as US Agent.
- Serve as a line manager: constructing and developing a team (as resources are assigned)
- Provide strategic, tactical, and operational direction and guidance for product’s pipeline and key regulatory milestones.
- Responsible for developing, executing, and maintaining the regulatory commitments and requirements for assigned programs.
- Stay abreast of regulatory agency regulations, directives, guidelines and policies, etc. that could have an impact on product development to assess approval pathways and issues.
- Identify and communicate all issues to management related to product development that could impact product submission, approval, and product launch.
- Set and monitor submission timelines along with other key stakeholders.
- Facilitate and lead all communications with Regulatory Agencies / Health Authority as applicable.
- Ensure communication with the regulatory body is in accordance with established procedure within the department.
- At times, there may be the need for other functional areas to have a discussion with the Health Authority with their counterparts at the regulatory agency. The Regulatory Strategist/Lead should always be the point of contact and lead this interaction.
- Ensure that communication is documented per established procedure should be distributed within the Global Regulatory Affairs team and any other external department that is directly affected by the communication.
- Must be involved in writing, or to facilitate the authoring of certain regulatory sections of product submissions.
- Develops and manages relationships with external regulatory agencies, industry groups and business partners.
- As applicable, shall review the audit reports, Regulatory Agency inspection reports and responses to the inspection observations if any, when received
- To compile, prepare, and review regulatory submissions to regulatory agencies as applicable.
- Conduct department level training, as necessary, to educate regulatory strategists and other roles in the department on regulatory requirements, policies, and procedures.
- Participate in authoring and/or reviewing of the departmental procedure as applicable
Qualifications
- Extensive global regulatory leadership as demonstrated by experience (> 15 years), milestones reached (e.g., original/supplemental approvals, expedited program designations), and health authority engagements (e.g., FDA, EMA, and others)
- Strong staff and organizational development experience (e.g., building teams, and coaching and training both new and experienced staff); demonstrated strengths in delegation, resource allocation, and workload prioritization.
- Broad experience in and across regulatory disciplines (notably global/regional strategy, labeling, clinical, nonclinical, CMC)
- Direct experience and expertise in authoring and filing regulatory documentation across major regulated markets
- Ability and interest in building and/or working a nimble resourcing environment
- Advanced degree (MD, PhD, PharmD, JD, MS, MBA) preferred
Location
- East coast, with intermittent travel to New Jersey (Princeton), as needed or upon request
This position is part of the Annual Performance Bonus Plan, and may be eligible for the Long Term Incentive Plan . Employees are eligible to participate in Company employee benefit programs which include medical, dental and vision coverage; life insurance; disability insurance; 401(k) savings plan; flexible spending accounts; and the employee assistance program. Employees also receive various paid time off benefits, including vacation time and sick time.
The compensation and benefits described above are subject to the terms and conditions of any governing plans, policies, practices, agreements, or other materials or documents as in effect from time to time, including but not limited to terms and conditions regarding eligibility. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company, or individual department/team performance, and market factors.
The preceding job description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of the incumbent(s).
We provide equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, military or veteran status, generic predisposing characteristics or any other basis prohibited by law.
Notice to Agency and Search Firm Representatives:
Sun Pharmaceuticals (Sun) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Sun employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Sun. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral.
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Princeton, New Jersey, United States Sun Pharmaceutical Industries, Inc. Full timeJob Summary We are seeking a highly experienced Senior Director, Global Regulatory Portfolio Lead to join our team at Sun Pharmaceutical Industries, Inc. This is a key leadership role that will provide strategic direction and guidance for the development and implementation of global registration pathways for our products. The successful candidate will have a...
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Princeton, New Jersey, United States Sun Pharmaceutical Industries, Inc. Full timeThe Senior Director, Global Regulatory Portfolio Lead, will provide leadership for the regulatory strategy of one or more in-line and pipeline assets in one or more therapeutic areas. This role will be a key member of the Global Regulatory Affairs Leadership Team, reporting directly to the VP/Head, GRA. The successful candidate will serve as a key corporate...
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Princeton, New Jersey, United States Sun Pharmaceutical Industries, Inc. Full timeJob SummaryThe Senior Director, Global Regulatory Portfolio Lead will provide leadership for the regulatory strategy of one or more in-line and pipeline assets in one or more therapeutic areas. This role will be a key member of the Global Regulatory Affairs Leadership Team, reporting directly to the VP/Head, GRA.Key Responsibilities Serve as key corporate...
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