Ccrps
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
CDISC implementation expertise
Advanced degree in a 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 years of experience, skillset, geographic location, 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.
$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 diagnostics company whose vision is to transform cancer care for patients all over the world. We empower clinicians with the high‑value insights they need to guide and assure patients at pivotal moments in the race to diagnose and treat cancer. Our Veracyte Diagnostics Platform delivers high‑performing cancer tests that are fueled by broad genomic and clinical data, deep bioinformatic and AI capabilities, and a powerful evidence‑generation engine, which ultimately drives durable reimbursement and guideline inclusion for our tests, along with new insights to support continued innovation and pipeline development. For more information, please visit www.veracyte.com or follow us on LinkedIn or X (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 careers@veracyte.com
PI280137035
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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
CDISC implementation expertise
Advanced degree in a 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 years of experience, skillset, geographic location, 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.
$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 diagnostics company whose vision is to transform cancer care for patients all over the world. We empower clinicians with the high‑value insights they need to guide and assure patients at pivotal moments in the race to diagnose and treat cancer. Our Veracyte Diagnostics Platform delivers high‑performing cancer tests that are fueled by broad genomic and clinical data, deep bioinformatic and AI capabilities, and a powerful evidence‑generation engine, which ultimately drives durable reimbursement and guideline inclusion for our tests, along with new insights to support continued innovation and pipeline development. For more information, please visit www.veracyte.com or follow us on LinkedIn or X (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 careers@veracyte.com
PI280137035
#J-18808-Ljbffr