Senior Manager, Clinical Data Management
$164k - $200kDeciphera Pharmaceuticals
Company Description
Deciphera, a member of Ono Pharmaceutical Co., Ltd., is a biopharmaceutical company focused on discovering, developing, and commercializing important new medicines and providing hope to people living with cancer, neurologic and autoimmune disease. The spirit of collaboration that has brought medications to life continues to guide how we operate, grow, and discover new breakthroughs. We cultivate an inclusive culture that values curiosity, creativity, and shared accountability—empowering individuals to challenge the unknown together. Learn more about Deciphera, a member of Ono Pharmaceutical Co., Ltd., by visiting our website:
Job Description
The Senior Manager, Clinical Data Management (CDM) leads data management activities for clinical studies or clinical programs, ensuring high standards of data quality and integrity. This role may serve as lead CDM for multiple trials, with accountability for complex or pivotal studies. The position works closely with internal stakeholders and external vendors to deliver high-quality clinical data on agreed timelines. The Senior Manager also supports inspection readiness and process improvement within the CDM function.
Key Responsibilities:
Clinical Data Management Leadership & Study Oversight
- Serve as lead CDM for multiple clinical trials
- Ensure data quality and data integrity for complex and/or pivotal clinical studies
- Oversee all activities outlined in the Data Management Plan (DMP)
- Develop data acquisition strategies and ensure supporting systems are validated and meet intended study needs
Vendor & Stakeholder Management
- Oversee outsourced CDM vendors and ensure performance aligns with Deciphera standards
- Participate in vendor selection and management
- Review vendor invoices as applicable
- Collaborate with cross functional team on data deliverables
Leadership, Process & Continuous Improvement
- Enhance CDM processes and strengthen cross functional collaboration
- Support department initiatives as needed
Inspection Readiness, Quality & Metrics
- Lead CDM inspection activities and manage findings to resolution
- Ensure CDM documentation is complete and filed in the TMF
Other duties and responsibilities as assigned
Qualifications
- Bachelor’s or master’s degree with 8+ years of experience in Clinical Data Management
- Effective communication, organizational, and project management skills
- Knowledge of FDA/CFR and ICH/GCP
- Familiarity with CDISC and CDASH standards
Preferred Capabilities:
- Experience leading complex or pivotal clinical trials
- Vendor oversight experience
- Inspection and audit support experience
Additional Information
Deciphera is committed to fair and equitable compensation practices. The base salary pay range for this role is $164,000 - $200,000. 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.
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.
Summary
- Type: Full-time
- Function: Science
- Experience level: Mid-Senior Level
- Industry: Pharmaceuticals
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