Deciphera Pharmaceuticals, Inc.

Manager, Regulatory Affairs

Deciphera Pharmaceuticals, Inc.$116K — $160K *
US-AnywhereRemote in Waltham, MA
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in a scientific field preferred.
  • 6+ years of experience in the pharmaceutical sector, with 4+ years in Regulatory Affairs.
  • Deep understanding of U.S. and international drug development regulations.
  • Exceptional verbal and written communication and organizational skills.
  • Proven ability to thrive in a high-paced, self-motivated environment.
  • Experience in supporting initial INDs/CTAs and marketing applications is a plus.

Responsibilities

  • Prepare, review, and submit regulatory filings such as INDs/CTAs, amendments, and Orphan drug applications.
  • Coordinate the creation of documents for meetings with global health authorities.
  • Contribute to the development of global regulatory strategies and ensure compliance with quality standards.
  • Represent regulatory interests in global study-level activities throughout the trial lifecycle.
  • Collaborate with external partners on regulatory submissions and activities.
  • Support ongoing regulatory operations and improvement projects, including SOP development.

Benefits

  • Competitive salary with annual bonus opportunities.
  • Comprehensive medical, dental, and vision insurance packages.
  • 401(k) retirement plan with company matching.
  • Generous parental leave and family planning support.
  • Strong organizational culture with personal and professional growth opportunities.
Full Job Description
We are seeking an experienced regulatory professional to support global regulatory activities across early- and late-stage development programs through lifecycle management. The Manager, Regulatory Affairs will partner cross-functionally to support high-quality regulatory submissions and help drive successful interactions with global health authorities.

This role will support regulatory strategy and execution for submissions including INDs, CTAs, NDA components, supplements, and other product-related regulatory activities. The ideal candidate brings strong knowledge of U.S. and international regulatory requirements, excellent collaboration skills, and the ability to manage multiple priorities in a fast-paced environment.

Key Responsibilities
  • Support preparation, review, and submission of regulatory filings including INDs/CTAs, amendments and information requisitions, Orphan drug applications, Annual Reports, and Investigator's Brochures.
  • Assist in coordination and preparation of global health authority meeting documents.
  • Contribute to global regulatory strategy and ensure submissions meet health authority requirements and quality standards.
  • Represents regulatory for global study-level regulatory activities included but not limited to study start-up, study maintenance, and end of trial activities.
  • Collaborate with external partners and vendors on regulatory activities and submission support.
  • Support regulatory operations and continuous improvement initiatives, including work instruction and SOP development and maintenance.


Qualifications

Qualifications
  • Bachelor's degree, preferably in a scientific discipline.
  • 6+ years of pharmaceutical industry experience, including 4+ years in Regulatory Affairs.
  • Strong knowledge of U.S. and international regulatory requirements for drug development.
  • Excellent verbal and written communication, organizational, and cross-functional collaboration skills.
  • Strong experience in a self-motivated, fast-paced environment
  • Experience supporting initial INDs/CTAs, and initial marketing application activities is highly desirable.


Additional Information

Deciphera is committed to fair and equitable compensation practices. The base salary pay range for this role is $116,000 - $160,000. Actual compensation packages will depend on various factors, including, but not limited to depth of experience, education, skillset, overall performance and/or location.

Deciphera believes in providing a competitive compensation and benefits package to all employees. Our base salary is just one component of Deciphera's competitive total rewards strategy that also includes annual performance bonus, a long-term incentive plan, full range of benefits and other incentive compensation plans (if applicable)

Benefits:
  • Competitive salary and annual bonus.
  • Comprehensive benefits package including medical, dental, vision insurance, 401(k) retirement plan with company match, and more.
  • Generous parental leave and family planning benefits.
  • Outstanding culture and opportunities for personal and professional growth.

About Deciphera Pharmaceuticals, Inc.

Deciphera Pharmaceuticals is a clinical-stage biopharmaceutical company focused on discovering, developing and commercializing innovative medicines to improve the lives of cancer patients. The company's drug candidates include ripretinib, a broad-spectrum KIT and PDGFR? inhibitor, and DCC-3014, a selective inhibitor of CSF1R. Ripretinib is in clinical development for the treatment of gastrointestinal stromal tumors (GIST), systemic mastocytosis (SM), and other solid tumors. DCC-3014 is in Phase 1 clinical development for the treatment of solid tumors. Deciphera Pharmaceuticals is headquartered in Waltham, Massachusetts.
Learn more about Deciphera Pharmaceuticals, Inc.
Size
280 employees
Market Cap
$1 billion
Industry
Net Income
-$266.4 million
Founded
2003
Revenue
$42 million
NASDAQ

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