Sr Mgr, Program Mgmt BU Evidence

Edwards Lifesciences Gruppe; Irvine (CA); On-site; USD 139,000 - 196,000; Full time

Benefits offered by this job

Competitive salaries

Performance-based incentives

Benefits programs

Job summary

Edwards Lifesciences is seeking a Sr. Manager for the PMO within the Transcatheter Mitral and Tricuspid Therapies (TMTT) division in Irvine, CA. You will lead cross-functional clinical trial programs, drive planning, risk management and delivery of key objectives.

This onsite role emphasizes collaboration with clinical, regulatory, marketing, and operations teams to advance patient-focused programs. The position requires a bachelor’s degree with extensive project management experience (PMP

Qualifications

• Bachelor's Degree with 10+ years managing mid-to-large scale projects or equivalent.
• Master’s Degree with 8+ years of experience or equivalent per Edwards criteria.
• PMP training and certification strongly preferred.

Responsibilities

• Develop multi-level, detailed project plans to meet clinical, medical and regulatory objectives.
• Lead cross-functional core teams, ensuring consensus and accountability.
• Manage scope, risks, and changes to deliver successful trial programs.
• Analyze performance to plan and develop corrective actions for variances.
• Report progress with dashboards and weekly status updates.
• Coordinate resources with functional leads to support program objectives.
• Communicate with senior stakeholders to align strategy and priorities.

Skills

Project management

Cross-functional leadership

Stakeholder communication

Risk management

Leadership

Education

Bachelor's Degree (min 10 years)

Master's Degree (8 years)

Tools

MS Office Suite

PM software

Job description

Sr. Manager, Project Management BU PMO, Evidence, TMTTMake a meaningful difference to patients around the world. Our project management teams support many parts of Edwards, including Engineering, HR, Marketing, IT, and more. You’ll be a trusted thought leader as you ensure our projects are completed efficiently and effectively. Your strategic mindset and fresh perspectives will be an essential part of how we bring innovative solutions for patients.Patients with mitral and tricuspid heart valve disease often have complex conditions with limited treatment options. Our Transcatheter Mitral and Tricuspid Therapies (TMTT) business unit is boldly pursuing an innovative portfolio of technologies to address a patient’s unmet clinical needs. It’s our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey.Edwards has a unique opportunity to join the Transcatheter Mitral and Tricuspid Therapies (TMTT) division. As a Manager in the Clinical, Medical, and Regulatory Affairs Program Management Office, you will lead multiple cross-functional clinical trial programs and teams to plan, execute and drive business objectives.Work Schedule: This is an onsite position in Irvine, CA.How you’ll make an impact:Planning: Develop multi-level, detailed project plans to meet clinical, medical and regulatory objectives based on cross-functional input and analysis. Build core team consensus and team ownership of the plan.Scope: Understanding of product development process, clinical trial milestones, and strategic objectives to drive a successful trial program.Determines and discerns requirements on large scale projects to establish project and program deliverables. Manages changes to the project scope and schedule, anticipates risks, builds various scenarios to drive decision making and agility.Performance Measurement and Risk Mitigation: Analyze performance to plan and develop corrective action plans for any variances with the core team. Identify forward looking risk and determine mitigation plans with core leadership team.Team Leadership: Lead cross-functional core team meetings. Build the following within the team: meeting discipline (agenda, minutes, action items) and team esprit de corps, problem solving culture and accountability.Resource Management: Partner with functional leads, cross-functional team members and other project managers to define/manage resource requirements to support program objectives.Communication and Reporting: Maintain weekly status reports, timelines, and program level dashboards. Proactively initiate efficient and effective communication, influence strategic discussions drawing on clinical knowledge, and provide clarity for roles and responsibilities to align stakeholders. Serve as conduit between project/team members in all cross-functional groups (e.g. Clinical, Marketing, Ops, Quality, R&D, Regulatory, Finance, Strategy, etc.)Strategy: Serve as a PMO lead in strategic conversations with senior internal and external personnel to inform business planning and strategy, and represent cross-functional team.What you'll need (Required):Bachelor's Degree with minimum 10 years hands on experience required in related field, managing mid-to-large scale projects or equivalent work experience based on Edwards criteriaOR Master’s Degree with 8 years of experience or equivalent work experience based on Edwards criteriaWhat else we look for (Preferred):Clinical trial experience, particularly within the medical device industryCompletion of project management training (PMP) strongly preferredProficient with MS Office Suite and related project management systemsExcellent documentation and communication skills and interpersonal relationship skills including negotiating and relationship management skills with ability to drive achievement of objectivesSubstantial understanding and knowledge of principles, theories, and concepts relevant to program and portfolio managementAbility to quickly learn and adapt to new technologies, and dynamic, agile environment and teamsAbility to work independently and as an active member and leader of the teamAbility to address delicate situations, operate with tact and professionalism, and effectively manage conflict to maximize project team progressAbility to lead, motivate, and inspire teams to action to support business objectivesStrong problem-solving, organizational, analytical and critical thinking skillsAbility to interact with senior internal and external personnel on significant matters often requiring coordination between organizationsEffectively communicate orally and in writing to all project stakeholdersAdhere to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/controlAligning our overall business objectives with performance, we offer competitive salaries, performance-based incentives, and a wide variety of benefits programs to address the diverse individual needs of our employees and their families.For California (CA), the base pay range for this position is $139,000 to $196,000 (highly experienced).The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience). Applications will be accepted while this position is posted on our Careers website.Edwards is an Equal Opportunity/Affirmative Action employer including protected Veterans and individuals with disabilities.