Deciphera Pharmaceuticals

Regional Business Director - West

Deciphera Pharmaceuticals · Full Time · 7 days ago

Deciphera Pharmaceuticals

🌎 United States 💵 $202K - $278K per year ⭐ 10+ yrs exp 💼 Others

Lead a regional sales team to prepare for and execute the launch of tirabrutinib for R/R PCNSL patients. Partner with cross-functional stakeholders to develop regional business plans and foster a high-performing culture of accountability.

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Sr. Manager, GMP Quality Assurance

Deciphera Pharmaceuticals · Full Time · 9 days ago

Deciphera Pharmaceuticals

🌎 United States 💵 $138K - $190K per year ⭐ 10+ yrs exp 💼 Software Development

Lead batch release activities and provide GMP oversight for manufacturing and distribution partners to ensure global regulatory compliance. Manage quality systems including deviations, CAPAs, and change controls while mentoring junior QA staff.

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Sr. Manager, GMP Quality Assurance

Deciphera Pharmaceuticals · Full Time · 16 days ago

Deciphera Pharmaceuticals

🌎 United States 💵 $138K - $190K per year ⭐ 10+ yrs exp 💼 Software Development

Lead GMP Quality Assurance activities, including batch release, material disposition, and oversight of manufacturing and distribution partners. Manage quality systems such as deviations, CAPAs, and change controls while ensuring compliance with global FDA, EMA, and ICH regulations.

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Director, Commercial Manufacturing & Process Engineering

Deciphera Pharmaceuticals · Full Time · 25 days ago

Deciphera Pharmaceuticals

🌎 United States 💵 $184K - $253K per year ⭐ 10+ yrs exp 💼 Others

Lead commercial manufacturing operations and process engineering activities within an outsourced CDMO model. Oversee technical transfers, process optimization, and regulatory CMC strategy to ensure reliable product supply and compliance.

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Manager, Regulatory Affairs

Deciphera Pharmaceuticals · Full Time · a month ago

Deciphera Pharmaceuticals

🌎 United States 💵 $116K - $160K per year ⭐ 5-10 yrs exp 💼 Legal

The role involves supporting global regulatory activities and submissions, including INDs and CTAs, across early- and late-stage development programs. The manager will partner cross-functionally to drive successful interactions with global health authorities and maintain regulatory operations.

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Manager, Regulatory Affairs

Deciphera Pharmaceuticals · Full Time · a month ago

Deciphera Pharmaceuticals

🌎 United States 💵 $116K - $160K per year ⭐ 5-10 yrs exp 💼 Legal

The role involves supporting global regulatory activities and submissions, including INDs and CTAs, across early- and late-stage development programs. The manager will partner cross-functionally to drive successful interactions with global health authorities and maintain regulatory operations.

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Medical Science Liaison II, Great Plains

Deciphera Pharmaceuticals · Full Time · 3 months ago

Deciphera Pharmaceuticals

🌎 Canada 💵 $192K - $264K per year ⭐ 10+ yrs exp 💼 Healthcare

The Medical Science Liaison II will serve as a field-based scientific expert in oncology, building relationships with KOLs and healthcare professionals to provide evidence-based information on therapies. Key duties include engaging experts, supporting studies, delivering scientific presentations, and gathering clinical insights.

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Clinical Project Manager

Deciphera Pharmaceuticals · Full Time · 3 months ago

Deciphera Pharmaceuticals

🌎 United States 💵 $129K - $194K per year ⭐ 5-10 yrs exp 💼 Product

The Clinical Project Manager will lead the planning, execution, and delivery of clinical trials, managing small to mid-sized studies and supporting complex programs. This involves coordinating cross-functional teams and external partners to ensure trials meet quality, timeline, and budget expectations.

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Director, Biostatistics

Deciphera Pharmaceuticals · · 4 months ago

Deciphera Pharmaceuticals

🌎 United States 💵 $200K - $275K per year ⭐ 10+ yrs exp 💼 Others

The Director, Biostatistics will serve as the Study Statistician for drug development programs, providing statistical strategy from early development through regulatory submission. Key duties include designing studies, authoring SAPs, overseeing analyses, and supporting regulatory filings like INDs, NDAs, BLAs, and MAAs.

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