Senior Manager, Clinical Data Analytics

Posted 2 Days Ago
Be an Early Applicant
Irvine, CA, USA
In-Office
139K-196K Annually
Senior level
Healthtech • Pharmaceutical
The Role
Leads clinical safety analytics, including dashboard design, safety data reconciliation, regulatory reporting, data quality control, and signal detection support. Manages a safety analytics team, partners with biostatistics, clinical data management, medical safety, and engineering teams, and translates reporting needs into technical requirements. Oversees process improvement, talent development, stakeholder communications, and corrective actions while ensuring compliant and timely clinical safety reporting.
Summary Generated by Built In

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. 

How you’ll make an impact:

  • Own end-to-end design, validation, and maintenance of clinical safety dashboards and reports (AE/SAE trends, coding accuracy, reporting timeliness) for internal stakeholders and safety governance bodies (e.g., DSMB, Safety Review Committee)
  • Lead safety data reconciliation across clinical database, safety database, and central lab/vendor sources
  • Ensure regulatory-compliant and timely expedited/periodic safety reporting (e.g., DSURs, IND safety reports) in partnership with Pharmacovigilance/Regulatory
  • Manage a team responsible for safety data QC, dashboard build/maintenance, and ad hoc safety analytics requests
  • Partner with Biostatistics, Clinical Data Management, and Medical Safety on signal detection methodology and dashboard logic
  • Partner with cloud/data engineering teams to translate clinical/safety reporting needs into technical requirements (data model, refresh cadence, query performance) for dashboard consumption
  • Develop a robust talent development plan in alignment with functional growth strategies of the department
  • Develop and deliver comprehensive presentations and written communications on clinical operations and study developments to stakeholders and management
  • Identify issues and collaborate with appropriate team members to bring to resolution; determine root cause; recommend and lead the implementation of corrective actions, complex process development and process improvement solutions to optimize strategic imperatives

What you’ll need (Required):

  • Bachelor's Degree or equivalent in a related field, or equivalent work experience based on Edwards criteria
  • Demonstrated track record in people management, or equivalent work experience based on Edwards criteria

What else we look for (Preferred):

  • Experience in clinical safety/pharmacovigilance and regulatory aspects of medical device technology, or equivalent work experience based on Edwards criteria —
  • Proven successful project management and leadership skills with the ability to influence change
  • Demonstrated strong problem-solving, process improvement, analytical, and collaborative skills
  • Excellent communication skills and interpersonal relationship skills including negotiating and relationship management skills with ability to drive achievement of objectives
  • Expert understanding of forecasting, reporting and analytics while addressing issues with impact beyond own team based on knowledge of related disciplines
  • Expert understanding of related aspects of processes and/or systems
  • Proficiency in Python (e.g., pandas, NumPy) for clinical/safety data analysis, validation, and QC, with working knowledge of web app frameworks (e.g., Flask, Streamlit, Dash) used to build or extend the safety dashboard application
  • Experience with a validated clinical/safety database and dashboarding/BI tools (e.g., Tableau, Power BI, Spotfire)
  • Familiarity with MedDRA/WHO-DD coding conventions and working knowledge of ICH-GCP safety reporting requirements
  • Working knowledge of cloud-hosted data architectures (AWS preferred) and data lake concepts (ingestion, ETL/ELT, data cataloging) sufficient to partner effectively with engineering teams — not expected to build pipelines personally, but must be able to translate business/safety requirements into technical specs and validate outputs
  • Proven expertise in MS Office Suite, SharePoint, and ability to operate general office machinery
  • Strict attention to detail
  • Ability to interact professionally with all organizational levels and proactively escalate issues to appropriate levels of management in the organization
  • Ability to work and excel within a fast-paced, dynamic, and constantly changing work environment
  • Ability to frequently interact with customers and/or functional peer group managers, normally involving matters between cross-functional teams and the company; often leads a cooperative effort among members of a project team
  • Adhere 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/control
     

Aligning 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.

Skills Required

  • Bachelor's degree or equivalent in a related field, or equivalent work experience
  • Demonstrated track record in people management, or equivalent work experience
  • Experience in clinical safety, pharmacovigilance, and regulatory aspects of medical device technology
  • Project management and leadership skills with the ability to influence change
  • Strong problem-solving, process improvement, analytical, and collaborative skills
  • Excellent communication, interpersonal relationship, negotiating, and relationship management skills
  • Expert understanding of forecasting, reporting, and analytics
  • Expert understanding of related processes and systems
  • Proficiency in Python, including pandas and NumPy, for clinical and safety data analysis, validation, and quality control
  • Working knowledge of Flask, Streamlit, or Dash for safety dashboard applications
  • Experience with validated clinical or safety databases and dashboarding or business intelligence tools such as Tableau, Power BI, or Spotfire
  • Familiarity with MedDRA and WHO-DD coding conventions
  • Working knowledge of ICH-GCP safety reporting requirements
  • Working knowledge of cloud-hosted data architectures, preferably AWS, and data lake concepts including ingestion, ETL/ELT, and data cataloging
  • Expertise in Microsoft Office Suite and SharePoint
  • Strict attention to detail
  • Ability to interact professionally across organizational levels and escalate issues appropriately
  • Ability to work effectively in a fast-paced, dynamic, and changing environment
  • Ability to frequently interact with customers and cross-functional peer group managers
  • Ability to lead cooperative efforts among project team members
  • Ability to follow company rules, environmental health and safety requirements, and injury and pollution prevention measures

Edwards Lifesciences Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Edwards Lifesciences and has not been reviewed or approved by Edwards Lifesciences.

  • Healthcare Strength Health coverage is considered strong, with multiple plan choices, HSA options, and fertility support, and the company highlights holistic well‑being programs.
  • Retirement Support A company 401(k) match and well‑regarded retirement offerings add clear long‑term value to total compensation.
  • Equity Value & Accessibility An Employee Stock Purchase Plan with a discount and look‑back feature makes equity ownership accessible and enhances the total rewards package.

Edwards Lifesciences Insights

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The Company
HQ: Irvine, CA
13,687 Employees
Year Founded: 1958

What We Do

Edwards Lifesciences (NYSE: EW), is the global leader in patient-focused medical innovations for structural heart disease, as well as critical care and surgical monitoring. We thrive on discovery and expanding the boundaries of medical technology, serving patients in 100+ countries, with the help of our employees in areas including Clinical Affairs, Quality Engineering, Research & Development, Regulatory Affairs, Sales & Marketing, corporate functions and more. Our roots date back to 1958 when Miles Lowell Edwards, a retired engineer with a background in hydraulics and fuel pump operations, set out to build the first artificial heart. Edwards believed the heart could be mechanized and was encouraged by Dr. Albert Starr to focus on developing an artificial heart valve. After just two years, the first Starr-Edwards mitral valve was developed and successfully placed in a patient. This innovation spawned Edwards Laboratories. Miles’ fascination with healing the heart and helping patients with heart disease stemmed from his own experience with rheumatic fever as a teenager and continues to fuel our patient-first culture today. Today, we are as passionate about providing innovative solutions for people fighting cardiovascular disease as we have ever been. It's our Credo. It takes integrity, collaboration, innovation, and focus. We are leaders in the design and manufacture of tissue replacement heart valves and repair products as well as advanced hemodynamic monitoring. We partner with physicians to innovate products designed to help patients live longer, healthier, and more productive lives. Our work is both rewarding and a privilege. The importance of what we do defines our approach. We work together to create an environment where ideas can flourish and we provide our people with the resources, expertise and support to bring those ideas to life. For our legal terms and trademarks, please visit: https://www.edwards.com/legal/legal-terms

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