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 - Experience with clinical Vendor/CRO management experience
- CDISC implementation expertise
- Advanced degree in related field
Impact: This role directly contributes to improving patient outcomes by ensuring the highest quality clinical data management standards in diagnostic testing development and validation. The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Base pay is one part of the Total Package that is provided to compensate and recognize employees for their work, and this role may be eligible for additional discretionary bonuses/incentives, and restricted stock units. Veracyte is a multi-state employer, and this salary range may not reflect positions that work in other states. Pay range $175,000—$186,000 USD What We Can Offer You Veracyte is a growing company that offers significant career opportunities if you are curious, driven, patient-oriented and aspire to help us build a great company. We offer competitive compensation and benefits, and are committed to fostering an inclusive workforce, where diverse backgrounds are represented, engaged, and empowered to drive innovative ideas and decisions. We are thrilled to be recognized as a 2024 Certified Great Place to Work in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose. About Veracyte Veracyte (Nasdaq: VCYT) is a global genomic diagnostics company that improves patient care by providing answers to clinical questions, informing diagnosis and treatment decisions throughout the patient journey in cancer and other diseases. The company’s growing menu of genomic tests leverage advances in genomic science and technology, enabling patients to avoid risky, costly diagnostic procedures and quicken time to appropriate treatment. The company’s tests in lung cancer, prostate cancer, breast cancer, thyroid cancer, bladder cancer and idiopathic pulmonary fibrosis are available to patients and its lymphoma subtyping and renal cancer tests are in development. With Veracyte’s exclusive global license to a best-in-class diagnostics instrument platform, the company is positioned to deliver its tests to patients worldwide. Veracyte is based in South San Francisco, California. For more information, please visit and follow the company on X (Formerly Twitter). Veracyte, Inc. is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability status. Veracyte participates in E-Verify in the United States. View our CCPA Disclosure Notice. If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to [email protected]
Job Tags
Interim role, Work at office, Worldwide,