Headquartered in Carlsbad, California, and with offices in Boston, Massachusetts, and Dublin, Ireland, Ionis has been at work for more than three decades discovering medical breakthroughs that have redefined life for people with serious diseases. We are pioneers in RNA-targeted medicines, and our platform continues to revolutionize drug discovery and transform lives for patients with unmet needs.  With five currently marketed medicines for serious diseases and an expansive late-stage pipeline, we continue to build upon our groundbreaking innovations in science and technology to provide greater value to patients; and we are well positioned financially to deliver on our strategic goals.

At Ionis, we pride ourselves on cultivating a challenging, motivating and rewarding environment that fosters innovation and scientific excellence. We know our success is a direct result of the exceptional talent and dedication of our employees.

With an unprecedented opportunity to change the course of human health, we look to add diverse individuals, skill sets and perspectives to our exceptional team. We continue to invest time, money, and energy into making our onsite and remote work environments a place where solid and lasting relationships are built and where our culture and employees can thrive.

We are building on our rich history, and believe our greatest achievements are ahead of us.  We invite you to apply and join us if you’re passionate about the opportunity to have meaningful impact on patients in need, our employees, and our organization.  Experience and contribute to our unique culture while you develop and expand your career!

 

DIRECTOR OF REGULATORY AFFAIRS - GLOBAL REGULATORY LEAD

SUMMARY:

Director of Regulatory Affairs will lead the commercial regulatory strategy for Ionis’ first-ever wholly owned commercial program.  This is an individual contributor role, reporting to the Executive Director, Regulatory Affairs. This position will work within cross-company development and commercial project teams, providing expert strategic regulatory plans, contributing to high-quality sNDA and MAA filings and responses, and contributing to the life-cycle commercial regulatory compliance. This individual will implement these plans through coordination, authorship and development of domestic and international drug applications and submissions, and through global regulatory agency interactions.  Experience with cardiovascular targeted therapeutics is a plus.  Experience as a commercial regulatory lead is strongly preferred.  This position may be fully remote, however preference will be given to San Diego-based applicants.  

RESPONSIBILITIES:

Formulates and implements creative and robust regulatory strategies and activities needed to secure approval of new drugs and indications and ensure life-cycle maintenance and compliance. Serves as primary communicator with FDA and other regulatory authorities building effective relationships; communicates outcomes to senior management as appropriate. Provides regulatory advice to other functional areas and serves as key regulatory interface with the Project and Commercial Brand Teams.  Provides technical review of data or reports that will be incorporated into regulatory submissions to ensure scientific rigor, accuracy, and clarity of presentation. Authors and compiles high-quality FDA and Ex-US regulatory applications including sNDA, marketing authorization applications, annual reports, etc; Prepares information or responses as requested by regulatory agencies.  Leads preparations for, and participate in, meetings with regulatory agencies to ensure efficient drug approvals. Maintains relationships and collaborates with partners to drive high-quality submissions; Works with multiple business partners to support Ex-US commercialization efforts. Effectively coordinates with Regulatory Operations to ensure on-time preparation and publication of regulatory submission documents. Identifies relevant and emergent guidance documents, international standards, or consensus standards; provide interpretive guidance and ensure guidance is implemented into development planning and execution. Ensures regulatory documentation is maintained appropriately. Other duties as assigned.

REQUIREMENTS: 

Bachelor’s Degree required; advanced degree preferred At least 10 years of increasing Regulatory Affairs experience and responsibility Solid working knowledge of relevant domestic and global regulations and guidance Experience filing marketing authorization applications (MAA) and supplemental New Drug Applications (sNDA) preferred Experience as Global Regulatory Lead (GRL) for a commercial product preferred Exercise outstanding judgment in all areas of responsibility History of successful interactions with global regulatory authorities  Energetic, self-motivated and a hands-on professional with a strong work ethic Able to perform independently and think analytically and creatively to solve problems Ability to be a true team player working toward common goals Excellent communication and interpersonal skills required to enable optimal interactions both internally and externally  An ability to be productive and successful in an intense work environment Willing to travel domestically and internationally up to 15%

 

 

Please visit our website, http://www.ionis.com, for more information about Ionis and to apply for this position; reference requisition #IONIS003453

Ionis offers an excellent benefits package! Follow this link for more details: Ionis Benefits

Full Benefits Link: https://www.ionis.com/careers/working-at-ionis/#:~:text=to%20Applicants%C2%A0%C2%BB-,Benefits,-Employees%20are%20rewarded

The pay scale for this position is $171,606 to $231,000

NO PHONE CALLS PLEASE. PRINCIPALS ONLY

 Ionis Pharmaceuticals, Inc. and all its subsidiaries are proud to be EEO employers.