Senior Clinical Trials & Data Operations Analyst

Edwards Lifesciences; Irvine (CA); On-site; USD 92,000 - 130,000; Full time

Job summary

Edwards Lifesciences in Irvine, CA is seeking a Clinical Affairs professional to advance the clinical evidence supporting our therapies. You will work with investigators, medical professionals, patient groups and regulators to optimize study outcomes and access to our technologies.

Collaborating with study teams, you will assess data, develop training materials, and drive process improvements to shorten trial timelines while maintaining rigorous standards.

Qualifications

• Bachelor’s Degree in related field with 5 years of hands‑on clinical research experience.
• Experience in clinical trial management and regulatory interaction is preferred.
• Excellent written and verbal communication and strong analytical skills.

Responsibilities

• Identifying technical and data issues and collaborating with team members to resolve root causes.
• Analyzing clinical output of complex studies and providing high‑level summaries to stakeholders.
• Leading implementation of process improvements to optimize global trial workflows and information flow.
• Communicating risks and impacts to study core teams and milestones.
• Developing timeline assessments with clinical stakeholders to meet study deadlines.
• Creating training material content for clinical sites and field staff.
• Assessing knowledge gaps and determining training plans with management.

Skills

MS Office Suite

Communication skills

Problem solving

Trial management knowledge

KOL liaison

Education

Bachelor's Degree in related field

Tools

MS Project

MS Excel

Job description

Edwards Lifesciences in Irvine, CA is seeking a Clinical Affairs professional to advance the clinical evidence supporting our therapies. You will work with investigators, medical professionals, patient groups and regulators to optimize study outcomes and access to our technologies.

Collaborating with study teams, you will assess data, develop training materials, and drive process improvements to shorten trial timelines while maintaining rigorous standards.