Associate Director, Regulatory CMC

Deciphera Pharmaceuticals; Waltham (MA); Hybrid; USD 160,000 - 219,000; Full time

Job summary

Deciphera Pharmaceuticals is seeking an Associate Director in Regulatory, CMC to lead and execute CMC regulatory activities in drug development. The successful candidate will ensure high-quality regulatory submissions and contribute to projects involving oligonucleotide products. This hybrid role offers an engaging opportunity for professional growth in a dynamic environment focusing on cancer therapeutic development.

Benefits

Comprehensive benefits package including medical, dental, and vision insurance

401(k) retirement plan with company match

Generous parental leave and family planning benefits

Annual performance bonus

Outstanding culture and opportunities for growth

Qualifications

• 8+ years in CMC Regulatory Affairs essential.
• Experience leading regulatory submissions for clinical development.
• Strong knowledge of cGMP and ICH guidelines required.

Responsibilities

• Lead CMC regulatory activities and submissions worldwide.
• Guide teams on CMC documentation standards.
• Communicate with health authorities for regulatory matters.

Skills

Project Management

Regulatory Submission

Communication Skills

Attention to Detail

Education

B.S. in a scientific discipline

Advanced degree

Tools

eCTD

Job description

Job Description

We are seeking an Associate Director in Regulatory, CMC who can independently lead, contribute and execute on CMC regulatory activities in support of Deciphera’s studies across all stages of clinical drug development. The primary responsibility will be to generate high quality and compliant CMC regulatory submissions for global investigational applications, initially focusing on oligonucleotide products. This position will report to the Senior Director of CMC Regulatory and will be a hybrid role based out of our Waltham, MA office. Additionally, opportunities will include contributing to CMC regulatory activities in support of other Deciphera small molecule and biologics programs and studies across all stages of clinical drug development.

Job Description

We are seeking an Associate Director in Regulatory, CMC who can independently lead, contribute and execute on CMC regulatory activities in support of Deciphera’s studies across all stages of clinical drug development. The primary responsibility will be to generate high quality and compliant CMC regulatory submissions for global investigational applications, initially focusing on oligonucleotide products. This position will report to the Senior Director of CMC Regulatory and will be a hybrid role based out of our Waltham, MA office. Additionally, opportunities will include contributing to CMC regulatory activities in support of other Deciphera small molecule and biologics programs and studies across all stages of clinical drug development.

What You’ll Do

• Collaborate with CMC cross-functional team members to plan, write and review CMC sections of pertinent regulatory submissions (e.g., global clinical trial and marketing applications, briefing documents, responses to Health Authorities)
• Provide regulatory guidance to cross-functional team members on required content of Module 2/Module 3.
• Review documentation in support of CMC and QA activities for drug development programs
• Review and assess proposed CMC changes during drug development for regulatory impact and filing requirements
• Communicate with regulatory Health Authorities on project related matters
• Provide insight and guidance on implementation of current regulations with respect to the preparation and submission of CMC regulatory documentation
• Review industry guidance and pharmacopoeia updates to ensure cross functional alignment with current practices and regulations
  
  

Qualifications

• B.S. in a scientific discipline required, advanced degree a plus.
• Must have at least 8 years pharmaceutical industry experience in CMC Regulatory Affairs. Direct experience with development programs through registration strongly preferred.
• Demonstrated leadership and track record of regulatory submissions, including effective project management.
• Experience in preparing high quality CMC regulatory submissions (Module 2 and Module 3) for global investigational and marketing applications.
• Strong knowledge of current Good Manufacturing Practices (cGMP), biologics drug development regulations and guidelines including ICH, FDA, and EMA guidelines
• Knowledge of eCTD elements and structure
• Must have previous experience leading/supporting interactions with health authorities
• Proven ability to manage multiple projects, identify and resolve regulatory issues
• Attention to detail and ability to work independently as well as part of a team environment
• Excellent organizational and communication skills, both written and verbal
• Strong interpersonal skills and the ability to effectively work with others
  
  

Additional Information

Deciphera is committed to fair and equitable compensation practices. The base salary pay range for this role is $160,000 - $219,000. 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.
  
  

Apply Now: Join us in our mission to improve the lives of people with cancer. Apply today to become a part of our dynamic team!

EQUAL EMPLOYMENT OPPORTUNITY INFORMATION

Deciphera is committed to equal employment opportunity and values diversity. To ensure that we comply with reporting requirements, we invite you complete the confidential survey at the end of this application. Providing this information is optional. It will not be accessible or used in the hiring process, and has no effect on your opportunity for employment. This information will also be treated confidentially. We are committed to make all hiring decisions and other employment decisions on a non-discriminatory basis.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Science

• Industries

  Pharmaceutical Manufacturing

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