
Clinical Trial Operations Analyst
Edwards Lifesciences is looking for a Clinical Trial Operations Analyst to join our team! Our ideal candidate is highly organized and detail-oriented with a strong background in clinical trial operations. We are looking for a self-starter who can identify areas of improvement and develop solutions to ensure the success of clinical trials.The Clinical Trial Operations Analyst will be responsible for planning, designing, and executing clinical trials in a timely and cost-effective manner. The successful candidate will be a critical thinker and problem solver with an eye for detail. We are looking for someone who can work collaboratively with cross-functional teams to ensure compliance with applicable regulations and standards.To be successful in this role, the ideal candidate should have a degree in Life Sciences, Medical Sciences, or a related field, plus at least 2 years of experience in a similar role. They should also have a strong background in clinical trial operations, a working knowledge of applicable regulations, and experience with database management. An understanding of project management principles and proficiency in Microsoft Office applications is also necessary.We are looking for someone who is passionate about improving patient outcomes and eager to join a forward-thinking team. If you have the qualifications and the drive to make a positive impact, we want to hear from you!
Responsibilities:
- Plan, design, and execute clinical trials in a timely and cost-effective manner.
- Identify areas of improvement and develop solutions to ensure the success of clinical trials.
- Work collaboratively with cross-functional teams to ensure compliance with applicable regulations and standards.
- Utilize project management principles to ensure successful completion of clinical trials.
- Manage databases for clinical trials.
- Create reports to track progress of clinical trials.
- Monitor and assess progress of clinical trials.
- Develop strategies to improve patient outcomes.
- Maintain a working knowledge of applicable regulations.
- Utilize Microsoft Office applications to complete tasks.
Or Related Field
Strong Organizational Skills And Attention To Detail
Excellent Written And Verbal Communication Skills
Bachelor's Degree In Life Science
Health Science
+ Years Of Experience In A Clinical Research Environment
Previous Experience In Clinical Operations And/Or Clinical Trial Management
Proficiency In Microsoft Office And Experience With Clinical Trial Management Systems
Knowledge Of Gcp And Ich Guidelines
Documentation
Quality Assurance
Process Improvement
Project Management
Data Analysis
Communication
Attention to detail
Problem Solving
Critical Thinking
Regulatory compliance
Stakeholder management
Operational excellence
Clinical Trials
Medical Writing
Protocol Development
Communication
Leadership
Negotiation
Problem Solving
Time management
Interpersonal Skills
creativity
self-motivation
Teamwork
Adaptability
According to JobzMall, the average salary range for a Clinical Trial Operations Analyst in Irvine, CA, USA is $54,000 - $96,000 per year. This range can vary depending on the experience and qualifications of the individual.
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Edwards Lifesciences (NYSE: EW) is the global leader in the science of heart valves and hemodynamic monitoring.

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