Deciphera Pharmaceuticals, Inc.

Vice President, Pharmacovigilance

Deciphera Pharmaceuticals, Inc.$335K — $460K *
Pharmaceuticals & Biotech
11 - 15 years of experience
Job Overview by Ladders

Qualifications

  • MD, DO, PharmD, PhD, or equivalent advanced scientific or healthcare degree.
  • 15+ years of experience in pharmacovigilance or drug development in biotech or pharmaceutical sectors.
  • 8+ years of leadership experience in managing global pharmacovigilance or clinical safety organizations.
  • Experience with products across clinical development and commercialization phases.
  • Broad understanding of global pharmacovigilance regulations and best practices.
  • Demonstrated expertise in safety governance and risk management.
  • Strong stakeholder management and strategic communication skills.

Responsibilities

  • Develop and execute global pharmacovigilance strategy in line with corporate goals.
  • Lead safety governance, surveillance, and risk management for products.
  • Act as a senior safety advisor to executive leadership and committees.
  • Ensure compliance and quality in global pharmacovigilance activities.
  • Establish scalable pharmacovigilance systems and operational capabilities.
  • Build and nurture a high-performing pharmacovigilance organization.

Benefits

  • Competitive salary and annual bonus.
  • Comprehensive medical, dental, and vision insurance.
  • 401(k) retirement plan with company match.
  • Generous parental leave and family planning benefits.
  • Opportunities for personal and professional growth.
Full Job Description
We are seeking a strategic and accomplished Vice President, Pharmacovigilance to lead Deciphera's global drug safety and pharmacovigilance function. This executive leader will be accountable for patient safety, regulatory compliance, and proactive benefit-risk assessment across investigational and marketed products. The VP will set the vision for safety governance, product safety strategy, risk management, regulatory safety support, and pharmacovigilance operations while partnering closely across Clinical Development, Regulatory Affairs, Medical Affairs, Quality, Commercial, Technical Operations, and other key functions.

What You'll Do
  • Develop and execute the global pharmacovigilance strategy in alignment with corporate objectives, regulatory requirements, and Deciphera's commitment to patient safety.
  • Provide executive leadership for benefit-risk evaluation, safety governance, safety surveillance, signal management, and risk management across investigational and marketed products.
  • Serve as a senior safety advisor to executive leadership and represent Pharmacovigilance in governance committees, leadership forums, and interactions with health authorities.
  • Ensure global pharmacovigilance activities are compliant, inspection-ready, scientifically rigorous, and aligned with applicable regulatory requirements, GCP standards, and internal quality systems.
  • Establish and evolve scalable pharmacovigilance systems, processes, quality frameworks, vendor partnerships, and operational capabilities to support a growing global portfolio.
  • Build, develop, and lead a high-performing pharmacovigilance organization while fostering a culture of scientific excellence, accountability, collaboration, and patient-focused decision making.


Qualifications
  • MD, DO, PharmD, PhD, or equivalent advanced scientific or healthcare degree.
  • 15+ years of progressive experience in pharmacovigilance, clinical safety, drug safety, or drug development within the biotechnology or pharmaceutical industry.
  • 8+ years of leadership experience managing global pharmacovigilance, clinical safety, or patient safety organizations.
  • Demonstrated experience supporting products across clinical development and commercialization.
  • Deep understanding of global pharmacovigilance regulations, guidelines, and industry best practices, including FDA, EMA, ICH, GCP, and other applicable requirements.
  • Experience with safety governance, benefit-risk assessment, signal detection, risk management, safety reporting, and inspection readiness.
  • Track record of successful health authority interactions, regulatory inspections, audits, and cross-functional safety leadership.
  • Strong strategic leadership, communication, decision-making, and stakeholder management skills.

Preferred Experience
  • Oncology experience strongly preferred.
  • Experience supporting small molecule therapeutics.
  • Prior experience leading pharmacovigilance activities for commercial-stage products.
  • Experience working in a global, outsourced operating model utilizing CROs and external pharmacovigilance vendors.
  • Demonstrated success building, scaling, and evolving pharmacovigilance organizations, systems, and operating models.
  • Experience supporting regulatory submissions, product launches, and post-marketing safety activities in multiple global markets.
  • Strong business acumen with the ability to align safety strategy with corporate objectives.


Additional Information

Additional Information

Deciphera is committed to fair and equitable compensation practices. The base salary pay range for this role is $335,000-$460,000. 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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