CareDx, Inc. is a leading precision medicine solutions company focused on the discovery, development, and commercialization of clinically differentiated, high-value healthcare solutions for transplant patients and caregivers. CareDx offers products, testing services, and digital healthcare solutions along the pre- and post-transplant patient journey, and is the leading provider of genomics-based information for transplant patients.
The Sr Director, PM lead is accountable for leading a high-impact team of Senior Program/Project Managers, and driving the successful execution of complex, enterprise-wide initiatives. This pivotal role requires a unqiue blend of operational rigor, strategic insight and deep biotechnological acumen. As a strategic partner in product and portfolio management, the PM Lead ensures technical delivery and drives long-term business growth while fostering a culture of transparency, excellence, and disciplined execution.
Responsibilities:
Leadership and Oversight of Senior Program Managers
- Direct Management: Lead, mentor, and supervise senior program managers, ensuring alignment with company goals and PMO best practices.
- Performance Evaluation: Set performance objectives, conduct regular reviews, provide feedback, and foster professional growth within the team.
- Resource Allocation: Strategically assign program managers to projects based on individual strengths, workload, and organizational priorities.
- Talent Development 1: Coach and upskill the PMO team in advanced program/portfolio management fundamentals and long-term strategic analysis
- Talent Development 2: Champion talent growth by crafting individual career plans and sourcing strategic opportunities to accelerate the professional trajectory of the Program Management team.
Program Oversight and Execution
- Strategic Program Management: Drive execution of complex, large-scale programs, ensuring alignment with business milestones, budgets, and regulatory requirements.
- Strategic Thought Partnership: Operate as a key collaborator in product development and portfolio optimization to ensure technical delivery remains synchronized with the company’s broader growth strategy.
- Risk Management: Identify potential risks and develop mitigation plans for high-impact programs, particularly those involving clinical trials, R&D, or regulatory submissions.
- Stakeholder Communication: Serve as the primary liaison for stakeholders, cross-functional teams, and external partners regarding program status, risks and achievements.
- Executive Reporting: Leverage real-time dashboards and performance KPIs to facilitate executive-level decision-making and portfolio optimization.
- Change Management: Lead organizational change initiatives tied to major programs, ensuring smooth transitions and adoption of new processes or technologies.
PPMO Process Improvement and Governance
- Standardization: Develop, refine, and enforce PPMO methodologies, tools, and templates to ensure consistency across projects.
- Quality Assurance: Conduct regular project health checks to ensure compliance with internal methodologies and financial reporting standards.
- Audits: Facilitate quarterly process audits and post-implementation reviews to surface improvement needs.
- Metrics and Reporting: Define and track key performance indicators (KPIs) for project and program success, preparing executive-level reports.
- Compliance: Ensure all projects adhere to regulatory, quality, and ethical standards specific to the biotech industry.
- Budget Oversight: Measure value realization via portfolio budget oversight, variance tracking and routine review of project value assumptions.
- Center of Excellence (COE): Facilitate quarterly process audits and post-implementation reviews to surface performance data, improvements or strategic pivots
Collaboration and Cross-Functional Leadership
- Cross-Departmental Coordination: Facilitate collaboration between R&D, clinical, regulatory, manufacturing, and commercial teams to achieve program objectives.
- Executive Strategy Support: Assist executive leadership in strategic planning, portfolio management, and prioritization of initiatives.
- Resource allocation: Coordinate site-level project validation and prioritization based on available resources, lead site prioritization reviews and support training and rollout of PPMO processes.
Continuous Improvement and Innovation
- Process Optimization: Identify and implement continuous improvements for project/ portfolio management processes, leveraging industry best practices and innovative approaches.
- Technology Adoption: Evaluate and implement project management technologies to enhance efficiency and transparency.
- Data insights: Utilize data driven insights to inform service-design decisions, drive project progression and make timely recommendations for project/program success
Requirements:
- Education: Bachelor’s Degree in life sciences or related field
- Experience: 10+ years of progressive experience in project/ program management
Preferred requirements:
- Advanced degree (MS, MBA, PHD)
- PMP, Six Sigma or equivalent certification
Additional Details:
Every individual at CareDx has a direct impact on our collective mission to improve the lives of organ transplant patients worldwide. We believe in taking great care of our people, so they take even greater care of our patients.
Our competitive Total Rewards package for US Employees includes:
- Competitive base salary and incentive compensation
- Health and welfare benefits, including a gym reimbursement program
- 401(k) savings plan match
- Employee Stock Purchase Plan
- Pre-tax commuter benefits
- And more!
- Please refer to our page to view detailed benefits at https://caredx.com/company/careers
In addition, we have a Living Donor Employee Recovery Policy that allows up to 30 days of paid leave annually to a full-time employee who makes the selfless act of donating an organ or bone marrow.
With products that are making a difference in the lives of transplant patients today and a promising pipeline for the future, it’s an exciting time to be part of the CareDx team. Join us in partnering with transplant patients to transform our future together.
CareDx, Inc. is an Equal Opportunity Employer-vets/disabled, and participates in the E-Verify program.
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This is the anticipated base salary range for candidates who will work in Brisbane, California. 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, the 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. CareDx is a multi-state employer, and this salary range may not reflect positions that work in other states.
Top Skills
What We Do
CareDx: Transforming Transplant Patient Care Through Novel Surveillance Management Solutions
CareDx, Inc. is dedicated to improving the lives of organ transplant patients through non-invasive diagnostics. By combining the latest advances in genomics and bioinformatics technology, with a commitment to generating high quality clinical evidence through trials and registries, CareDx is at the forefront of organ transplant surveillance and pre-transplant HLA typing solutions.
NASDAQ:CDNA
About AlloSure®
AlloSure is the first and only non-invasive blood test that directly measures allograft injury and identifies the probability of active rejection to better manage kidney transplant patients. AlloSure is a clinical-grade, proprietary Next-Generation Sequencing (NGS) based test to detect donor-derived cell-free DNA (dd-cfDNA) in order to identify organ injury in kidney transplant recipients. AlloSure is analytically validated as a sensitive, specific, and precise measurement of dd-cfDNA. AlloSure detects active rejection (acute active ABMR, chronic active ABMR, or TCMR) with high accuracy, outperforms serum creatinine in kidney transplant recipients, and is highly sensitive in distinguishing ABMR from no ABMR. AlloSure is performed in the CareDx CLIA-certified laboratory.
http://www.allosure.com/
About AlloMap®
AlloMap Molecular Expression Testing is a non-invasive blood test used to aid in the identification of heart transplant recipients with stable allograft function who have a low probability of moderate/severe acute cellular rejection at the time of testing in conjunction with standard clinical assessment. AlloMap testing measures the expression levels of 20 genes from a blood sample. The combined expression of these genes is represented as an AlloMap test score. AlloMap is performed in the CareDx CLIA-certified laboratory and has been commercially available in the United States since 2005. AlloMap was cleared by the U.S. Food and Drug Administration in 2008 and was CE marked for the European Union in 2011. Use of AlloMap is also included in the International Society for Heart and Lung Transplantation (ISHLT) Practice Guidelines, published in August 2010, the worldwide standard for the care of heart transplant patients.
http://www.allomap.com/
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