Senior Manager, Clinical Supply Chain

The Senior Manager Clinical Supply Chain is responsible for the planning forecasting packaging labeling distribution and inventory management of investigational products supporting Decipheras global clinical development programs.

This role serves as a critical partner to Clinical Operations CMC Quality Assurance Regulatory Affairs and external vendors by ensuring supply continuity inventory accuracy regulatory compliance and timely study execution across complex global clinical trials. The successful candidate will independently manage study-level clinical supply activities from startup through closeout while collaborating across internal and external stakeholders to support the successful delivery of clinical programs. 

What Youll Do 

• Develop clinical supply plans forecasts inventory strategies and risk mitigation plans for global clinical studies. 

• Manage packaging labeling distribution and investigational product logistics from study startup through closeout. 

• Partner with CDMOs depots logistics providers packaging vendors and other external suppliers to support global study execution. 

• Utilize IRT systems to support inventory management reporting study execution and issue resolution. 

• Identify supply risks drive issue resolution and provide study teams with clear recommendations and execution plans. 

• Collaborate with Clinical Operations CMC Regulatory Affairs Quality Assurance and external partners to support successful study delivery 

• Contribute to process improvement initiatives operational best practices SOP development and cross-functional team effectiveness. 

Qualifications :

What Were Looking For 

• Bachelors degree in Life Sciences Supply Chain Engineering Business or a related field.

• 8 years of clinical supply chain clinical trial supply clinical materials management or clinical drug supply experience within biotechnology pharmaceutical CRO or CDMO environments.

• Demonstrated experience supporting global clinical studies from startup through closeout.

• Strong experience with clinical supply forecasting inventory planning packaging labeling and distribution.

• Hands-on experience with IRT/RTSM systems including inventory management reporting and study support.

• Experience managing external vendors including packaging providers logistics partners depots and clinical supply service providers.

• Proven ability to independently manage multiple studies and work effectively across cross-functional teams. 

Preferred Qualifications 

• Experience supporting large-scale global Phase III clinical studies. 

• Small molecule clinical development experience. 

• Sponsor-side biotechnology or pharmaceutical experience. 

• Experience supporting studies across North America South America Europe and Asia Pacific. 

• Experience with comparator sourcing temperature-controlled logistics and global distribution activities. 

Additional Information :

This position is hybrid based on-site in Waltham MA. 

Deciphera is committed to fair and equitable compensation practices. The base salary pay range for this role is $141300 - $194300. Actual compensation packages will depend on various factors including but not limited to depth of experience education skillset overall performance and location. 

Deciphera believes in providing a competitive compensation and benefits package to all employees. Our base salary is just one component of Decipheras competitive total rewards strategy that also includes annual performance bonus a long-term incentive plan a 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

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 making all hiring decisions and other employment decisions on a non-discriminatory basis.

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.

Remote Work :

No

Employment Type :

Full-time