Senior Analyst, Clinical Data Management
Company websiteedwards.com (Edwards Lifesciences, opens in new tab)
Base salary $108K to $153K
Employer-published annual base salary, USD. Advertised base range in Irvine, CA
You apply on the employer's own site. Six Figure Work does not handle applications.
- LocationIrvine, CA
- WorkplaceWorkplace not stated
- Status at last checkSource accepting applications when checked
- Last checked (2 h ago) · observed since
About this job
Imagine how your ideas and expertise can change a patient’s life. We generate extensive clinical evidence to demonstrate the effectiveness and safety of our innovations and how our products transform patients’ lives. As part of our Clinical Affairs team, you’ll hone your scientific curiosity and passion for evaluating data to increase access to pioneering technologies for patients in need. In close partnership with principal investigators, dedicated medical professionals, patient advocacy groups, and regulatory authorities, you will drive the evidence needed to optimize patient outcomes.
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 will make an impact:
- Creating complex metrics to identify trends in data and remediation, utilizing tools (e.g., systems, reports) to assess need for training and providing recommendations to improve data status during study conduct.
- Defining and specifying clinically complex data collection requirements (e.g., eCRFs, CRFs, edit checks and collection of external data) for assigned studies; including defining, performing, and coordinating user acceptance testing (e.g. test scripts and checklists) to ensure appropriate data are collected.
- Leading project management activities for multiple (multi-site and multi-cohort) projects to bring clinical studies on-line, including conducting project team meetings, establishing and maintaining project timelines, and communications to stakeholders.
- Developing and maintaining Data Management deliverables including data management plans (DMPs), training materials and user aids in compliance with regulations.
- Evaluating data errors and collection issues; providing guidance and recommendations to clinical team for resolution.
- Performing Site/User Administration to allow access to the database, ensuring all users are qualified to access data base; providing guidance on more complex access rights for users.
- Leading development and review of SOPs, work instructions, and associated documents for CDM, including recommending revisions and updates to SOPs, participating in the development of user training.
What you’ll need (Required):
- Bachelor’s Degree in related field with 5 years of previous related experience in clinical research including clinical data management and/or clinical data entry or equivalent work experience based on Edwards criteria.
- Experience with EDC (Electronic Data Capture) systems
What else we look for (Preferred):
- Experience with AI Tools (Copilot & Claude)
- Experience with study start-up, conduct, and close-out
- Proven expertise in Microsoft Office Suite
- Basic project management skills
- Excellent written and verbal communication skills and interpersonal relationship skills including negotiating and relationship management skills
- Excellent problem-solving and critical thinking skills
- Full knowledge and understanding of policies, procedures and guidelines relevant to clinical research
- Full knowledge of processes and procedures in clinical data management
- Full knowledge of protocols, DMPs, and SAPs
- Ability to manage competing priorities in a fast-paced environment
- Strict attention to detail
- Must be able to work in a team environment, including inter-departmental teams and key contact representing the organization on projects
- Ability to interact with senior internal and external personnel on significant matters often requiring coordination between organizations
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.
The base pay range for this position is $108,000 to $153,000 (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.
Source: Edwards Lifesciences on Workday · View original posting (opens in new tab)
This listingSenior Analyst, Clinical Data Management$108K to $153K
Senior Specialist, Clinical Research Monitoring$108K to $153K
Sr. Quality Engineer, NPD - IHFM$108K to $153K
Product Manager, Upstream Marketing TMVR Global Marketing$108K to $153K
Senior Engineer, Automation$108K to $153K
Senior Engineer, Product and Process Engineering$108K to $153K
Senior Specialist, Clinical Imaging, TMTT$108K to $153K
Chart as a table
| Role | Published base |
|---|---|
| Senior Analyst, Clinical Data Management (this listing) | $108K - $153K |
| Senior Specialist, Clinical Research Monitoring | $108K - $153K |
| Sr. Quality Engineer, NPD - IHFM | $108K - $153K |
| Product Manager, Upstream Marketing TMVR Global Marketing | $108K - $153K |
| Senior Engineer, Automation | $108K - $153K |
| Senior Engineer, Product and Process Engineering | $108K - $153K |
| Senior Specialist, Clinical Imaging, TMTT | $108K - $153K |
Observed changes
- First observed on the employer's board
- Began meeting the published-salary criteria
- Observed since
- Employer-stated posting date
- 2026-09-10
Where this pay comes from
Location as the employer wrote it: USA - California – Irvine
The base pay range for this position is $108,000 to $153,000 (highly experienced).
- Method
- Employer text, read with fixed rules and re-verified
- Checked
- Rule set
- us-base-v2
The pay passage appears in the employer's own job text. Fixed, deterministic rules located it, and the passage below was checked against the stored copy of the posting.
What we verified
- The pay figures come from the employer's own listing, quoted exactly above.
- The pay is an annual base salary in US dollars with a minimum of at least $100,000.
- The role was publicly listed on the employer's job board when last checked.
We do not verify what the employer will actually offer, whether the employer is still recruiting for the role, or anything beyond what the employer published. Full methodology.
