Analyst, Data Analytics TMTT

Edwards Lifesciences Gruppe

United States

On-site

USD 74,000 - 104,000

Full time

4 days ago
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Job summary

Edwards Lifesciences in the United States seeks a Clinical Affairs professional to drive evidence supporting innovative technologies. You will perform analyses for clinical trials, forecasting resource needs, and collaborate with investigators, medical affairs, and regulatory partners to optimize patient outcomes.

The role emphasizes quantitative methods, Excel/PowerPoint proficiency, and clear communication.

Qualifications

  • Bachelor's degree and 3+ years of related experience or equivalent
  • Experience in quantitative or analytical field
  • Experience in clinical research in medical devices is preferred
  • Proficiency with Excel and PowerPoint, and MS Office apps
  • Strong written and verbal communication and collaboration skills

Responsibilities

  • Perform analyses (enrollment, costing, resourcing) for clinical trials to forecast key stakeholders
  • Modify analysis tools using clinical models (inventory, headcount, site activations)
  • Organize, analyze and create reports and dashboards for moderately complex challenges
  • Lead portions of clinical projects with vendors and cross-functional teams
  • Identify and propose process improvements in clinical affairs

Skills

Clinical research
Machine learning
Excel
PowerPoint
MS Office
Communication skills
Data analytics
Quantitative methods

Education

Bachelor's degree

Job description

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.

What you will need (Required):

Bachelor's Degree and a minimum of 3 years related experience or equivalent work experience based on Edwards criteria Experience in quantitative or analytical field or equivalent work experience based on Edwards criteria

What else we look for (Preferred):

Experience working in clinical research in the medical device industry or equivalent work experience Experience with machine learning Proven expertise in Excel and PowerPoint and other MS Office Suite apps including Word and Access Good written and verbal communication skills and interpersonal relationship skills Good problem-solving, organizational, analytical and critical thinking skills Moderate knowledge and understanding of policies, procedures and guidelines relevant to data analytics within clinical trials Solid understanding of quantitative methodologies, techniques and tools Ability to manage competing priorities in a fast paced environment Ability to work in a team environment, including inter-departmental teams and representing the organization on specific projects

Perform analysis (e.g. enrollment, costing, resourcing) related to clinical trials to develop forecasting for key stakeholders (e.g. Clinical Affairs, Regulatory and Medical Affairs, Strategy, Global Supply Chain, Finance Investigate, assess and interpret clinical intel for strategic decision making to support business objectives, while proposing moderately complex solutions and recommendations Modify analysis tools by leveraging existing clinical models (e.g. inventory, case management, headcount trial enrollment and site activations/deactivations) while utilizing clinical trial knowledge Organize, analyze and create reports, and dashboards to summarize moderately complex challenges in clinical affairs projects, programs and/or initiatives Lead portions of clinical projects in collaboration with stakeholders (e.g. vendors, cross-functional teams) Identify and propose process improvements as it relates to clinical affairs (e.g. screening process, physician training)

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.

#LI-Onsite

For California (CA), the base pay range for this position is $74,000 to $104,000(highly experienced). The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience).

Edwards is an Equal Opportunity/Affirmative Action employer including protected Veterans and individuals with disabilities.

Edwards Lifesciences is the leading global structural heart innovation company, driven by a passion to improve patient lives. Through breakthrough technologies, world-class evidence and partnerships with clinicians and healthcare stakeholders, our employees are inspired by our patient-focused culture to deliver life-changing innovations to those who need them most.

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