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Principal, Clinical Programming, Surgical

Edwards Lifesciences

Irvine, CAHybridPosted 15 days ago$132,000 - $186,000/year
Full TimeSenior LevelBioinformatics & Data ScienceMedical Device
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Summary

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.

Job description

Dedicated to innovation, our Surgical business unit is focused on identifying and solving critical, unmet needs in cardiac surgery. In understanding the challenges of open-heart surgery, we partner with surgical teams to deliver modern technologies intended to enhance patients' quality of life and expand their potential treatment opportunities. 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:

  • Provide technical expertise in clinical programming functional area and lead in the development of clinical databases, and tools and programs for data validation checks, and clinical trial reporting in collaboration with key stakeholders
  • Lead cross functional teams in the design and delivery of complex functional modules and provide clinical programming expertise regarding clinical trials, protocols, and case report forms
  • Lead the development of specifications for systems and/or processes, system upgrades/enhancements and integration; and engage IT to deliver higher level support to users
  • Develop and present high level technical training to end-users, including providing guidance to lower-level Clinical Programmers in their training program development
  • Identify resource needs for database implementation and participate in the evaluation of external resources/vendors
  • Manage daily service providers' activities for outsourced systems and services used in clinical trials
  • Participate in the creation and revision of new or existing SOPs, work instructions, workflow, forms, and templates to ensure clinical systems and activities are in compliance with the regulatory and company requirements

What you will need (Required):

  • Bachelor's Degree and a minimum of 6 years experience in clinical research, data management, software programming or related field or equivalent work experience based on Edwards criteria
  • Extensive experience with EDC (Electronic Data Capture) systems; Medidata programming experience

What else we look for (Preferred):

  • Master's Degree and a minimum of 5 years experience in clinical research, data management, software programming or related field or equivalent work experience based on Edwards criteria OR a Ph.D. and a minimum of 2 years experience in clinical research, data management, software programming or related field or equivalent work experience based on Edwards criteria
  • Expert knowledge in creating new and maintaining existing Medidata custom functions in C# or SQL.
  • Proven successful project management skills
  • Proven expertise in both Microsoft Office Suite, including advanced Excel and CDM (Clinical Data Management) systems
  • Excellent documentation and communication skills and interpersonal relationship skills including negotiating and relationship management skills with ability to drive achievement of objectives
  • Good presentation and facilitation skills
  • Ability to translate technical information to cross-functional teams
  • Extensive knowledge of own area within the organization while contributing to the development of new concepts, techniques, and standards
  • Extensive knowledge and understanding of policies, procedures and guidelines relevant in the development of clinical databases
  • Extensive knowledge of processes and procedures in clinical data management
  • Extensive knowledge of relational databases, systems, and programming languages
  • Extensive knowledge of clinical programming as it relates to business processes
  • Ability to manage competing priorities in a fast-paced environment
  • Represents leadership on sections of projects within a specific area interfacing with project managers and team members

Requirements

  • Bachelor's Degree and a minimum of 6 years experience in clinical research, data management, software programming or related field or equivalent work experience based on Edwards criteria
  • Extensive experience with EDC (Electronic Data Capture) systems
  • Medidata programming experience

Benefits

  • Competitive Salaries
  • Performance-Based Incentives
  • Comprehensive Benefits Programs

Company overview

Edwards Lifesciences (NYSE: EW) is the leading global structural heart innovation company, driven by a passion to improve patient lives. Founded in 1958 and headquartered in Irvine, California, the company specializes in developing breakthrough technologies for cardiovascular diseases. As a pioneer in the medical device industry, Edwards focuses on transcatheter heart valves, surgical heart valves, hemodynamic monitoring systems, and vascular solutions. The company's patient-focused culture inspires its 16,000+ employees worldwide to deliver life-changing innovations that address complex heart health challenges. Edwards serves patients in over 100 countries through its comprehensive portfolio of products including the SAPIEN transcatheter heart valve system, INSPIRIS surgical valves, and advanced monitoring technologies. With a commitment to research and development, the company invests 17-18% of its revenue back into R&D efforts, maintaining its position at the forefront of structural heart innovation. Edwards Lifesciences has impacted over one million patients globally through its transformative medical technologies.

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