Role Description
The Associate Director, Regulatory Strategy will be responsible for developing and implementing regulatory strategies to secure global investigational and marketing applications for assigned product(s) in the assigned therapeutic area.
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Leads the Product Regulatory Sub team.
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Ensures strategic messaging and content of global regulatory dossiers.
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May serve as the primary regulatory interface with the Asset Strategy Team and sub teams.
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Proactively anticipates and mitigates regulatory risks.
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Ensures compliance with global regulatory requirements.
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Manages assets through all phases of development from pre-FIH through active life cycle management activities.
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Demonstrates an understanding of drug development and exhibits leadership behaviors consistent with level.
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Has direct experience with regulatory acceleration strategies, developing regulatory strategy, analyzing regulatory precedence, and operational excellence in execution of regulatory strategy.
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This role may lead a team of regulatory professionals.
Qualifications
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Bachelor’s degree in scientific discipline; advanced scientific degree preferred (PharmD, Ph.D, MD).
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Regulatory Affairs Certification is highly desirable.
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8+ years pharmaceutical industry experience, including 5+ years in Regulatory Affairs leadership roles; Global experience desired.
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Requires innovator drug development experience in the US and EU/UK/EEA. Experience in Asia PAC, a plus.
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Proven 5+ years in a strategic leadership role with strong project management skills.
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Experience working in a complex and matrix environment.
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Experience directly interfacing with health authorities in a major market.
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Experience in multiple phases of development is required.
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Experience in rare disease, immunology or oncology is highly desirable.
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Knowledge of the drug development process and global submission process.
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Knowledge of global regulatory guidance as they relate to the overall global regulatory strategy.
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Cross functional partnering skills, team-oriented and ability to influence outcomes are necessary skills in the environment.
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Excellent organizational, communication and time management skills needed to manage multiple ongoing projects simultaneously.
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Experience working within corporate partnerships is a plus.
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Must be able to innovate, analyze and solve problems with minimal supervision and attention to detail.
Requirements
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Location: Syndax’s corporate office is in New York, NY.
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This is a remote opportunity.
Benefits
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Total compensation and rewards package that is among the most competitive in the industry.
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Base pay is determined within a range based on several factors including market data, experience, qualifications, demonstrated skills, relevant education or training, travel requirements and internal equity.
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Overall package includes an equity offering, annual target bonuses, and an outstanding benefits program.
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The anticipated annualized salary range for this role is $195,000 - $220,000.
Company Description
Syndax Pharmaceuticals is a commercial-stage biopharmaceutical company advancing innovative cancer therapies. Highlights of the Company’s pipeline include a menin inhibitor for R/R acute leukemia and a monoclonal antibody that blocks the CSF-1 receptor for chronic graft-versus-host disease. Fueled by our commitment to reimagining cancer care, Syndax is working to unlock the full potential of its pipeline and is conducting several clinical trials across the continuum of treatment.
For more information, please visit
www.syndax.com
or follow the Company on
X
and
LinkedIn
.
Syndax Pharmaceuticals is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.