Senior Clinical Data Manager

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.

Aortic stenosis impacts millions of people globally, yet it often remains under-diagnosed and undertreated. Edwards’ groundbreaking work in transcatheter aortic heart valve replacement (TAVR) pioneered an innovative, life-changing solution for patients by offering heart valve replacement without the need for open heart surgery. Our Transcatheter Heart Valve (THV) business unit continues to partner with cardiologists and clinical teams to transform patient care with devices supported by clinical evidence. It’s our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey.

As the Senior Clinical Data Manager, you will translate clinical study business requirements into system requirements for the collection and management of data from clinical trials. Additionally, you will ensure the quality and integrity of data collected in clinical studies, maintain the privacy of patient data, and efficiently record and report safety-related issues.

The ideal candidate will reside in the Western United States region.

How you will make an impact:  

• Create complex metrics to identify trends in data and remediation, utilizing tools (e.g., systems, reports) to assess need for training and provide recommendations to improve data status during study conduct

• Define and specify 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.

• Lead 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.

• Develop and maintain Data Management deliverables including data management plans (DMPs), training materials and user aids in compliance with regulations

• Evaluate data errors and collection issues; provide guidance and recommendations to clinical team for resolution

• Perform Site/User Administration to allow access to the database, ensuring all users are qualified to access data base; may provide guidance on more complex access rights for users

• Lead 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.

• Other incidental duties assigned by Leadership

What you'll need (Required):

• Bachelor's degree and 5 years of previous related experience in clinical research including clinical data management and/or clinical data entry OR

• Associate degree or equivalent in a related field and 7 years of previous related experience in clinical research including clinical data management and/or clinical data entry

• Experience with Medidata Rave EDC (Electronic Data Capture

• Ability to travel up to 20% to the corporate office

What else we look for (Preferred):

• Proficiency in Microsoft Power BI. Experience using Power BI for data visualization and analysis. This includes the ability to create and manage ad hoc reports in Power BI to support clinical data management needs.

• Experience in clinical data programming, including building and maintaining databases, and performing data migration tasks to ensure seamless integration and accuracy of clinical data.

• Full knowledge of protocols, DMPs, SAPs, Database Specification, and Data Validation Specification

• Proven expertise in Microsoft Office Suite

• Advanced Excel skills (pivot tables and formulas)

• Project management skills and lead cross functional meetings

• Full knowledge of processes and procedures in clinical data management

• Excellent written and verbal communication skills and interpersonal relationship skills including negotiating and relationship manag