Sr. Manager, Clinical Data Management
Confirmed live in the last 24 hours
Veracyte
Compensation
$175,000 - $186,000/year
Job Description
At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven environment. This is what we call the Veracyte way – it’s about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions.
Our Values:
- We Seek A Better Way: We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer care
- We Make It Happen: We act with urgency, commit to quality, and bring fun to our hard work
- We Are Stronger Together: We collaborate openly, seek to understand, and celebrate our wins
- We Care Deeply: We embrace our differences, do the right thing, and encourage each other
The Position:
The Senior Manager, Clinical Data Management is responsible for leading all aspects of Clinical Data Management Operations at Veracyte, ensuring data integrity and quality for clinical studies. This is a hands-on leadership role that requires both technical expertise and strategic oversight of the complete data management lifecycle.
Key Responsibilities:
- Direct end-to-end clinical data management operations, from protocol design to database closure
- Develop and implement comprehensive data management plans, validation specifications, and quality control procedures
- Design and validate eCRF systems and edit checks aligned with protocol requirements
- Oversee database development, validation programming, and query management
- Establish data collection methods and quality standards in collaboration with Clinical Affairs, Data Analysis, and IT teams
- Manage vendor relationships and oversee EDC system implementation
- Create and monitor project timelines for interim and final database locks
- Generate key metrics reports and data analytics for clinical studies.
Who You Are:
- Bachelor's degree in Computer Science, Life Sciences, or related field
- 8+ years hands-on experience in IVD, Medical Device, or Pharmaceutical clinical data management
- Previous management experience as this role will have people leadership responsibilities
- Extensive knowledge of GCP and GCDMP and proficiency in the following:
- Programming languages (R, SAS)
- Database management (SQL, PL/SQL)
- EDC systems and clinical data management platforms (e.g. Medidata, Medrio)
- CTMS and eTMF platforms with strong preference for experience with Veeva Vault
- Sample management platforms (e.g. LabVantage)
- Microsoft Office Suite
Technical Expertise:
- CDISC/CDASH/SDTM/ADAM standards
- FDA guidelines and regulations
- Database validation and quality control processes
- Clinical trials
- Experience with Medidata
- Experience with Veeva Vault
- Experience with LabVantage
- Clinical trial data workflows
Leadership Competencies:
- Strategic project management across multiple studies
- Strong analytical and problem-solving capabilities
- Excellence in cross-functional team collaboration
- Clear communication of technical concepts to non-technical stakeholders
- Proactive issue identification and resolution
- Ability to work independently while maintaining team alignment
- Ability to build and lead a clinical data management team.
Preferred Qualifications:
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