Associate Analyst, Clinical Operations

Innovation starts from the heart. Our Advanced Technology (AT) teams harness the imagination, courage, and resourcefulness to think beyond what’s currently possible, and create solutions for patients many years into the future. If you’re an early-stage innovator, then Edwards AT team is the place for you to take the next steps in your career. We’ll give you the tools and resources you need to create groundbreaking innovations that shape the future of structural heart technology.

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.

The Associate Analyst, Clinical Operations team member will play a pivotal role in ensuring clinical operations deliverables and analytics are completed.

How you will make an impact:

• Identify, develop, recommend, and implement basic process development and process improvement solutions to optimize global trial workflow timelines, (e.g., device return aging issues, status of open device issues/queries, etc.) including analyzing clinical device data
• Using approved templates, draft, redline and negotiate contracts, including NDAs, letters of termination, clinical trial agreements, service agreements, statements of work, amendments, etc.
• Negotiate clinical contract budgets
• Work collaboratively with various departments in order to process contract related requests, including Edwards’ Legal and Compliance departments, Risk Management, study managers, field staff, and clinical group directors
• Collaborate with the site manager to send out study training in accordance with the study training matrix and ensure documents are received
• Review and ensure accuracy and completeness of clinical study documents ensuring GDP and performing quality checks with limited supervision with limited direction
• Organize and archive documents and data in eTMF (electronic trial master file) and/or CTMS (clinical trial management system) ensuring compliance with internal procedures and regulatory guidelines. 
• Other duties as assigned (e.g. audit support, clinical payments, etc.)

What you will need (Required):

• Bachelor's Degree
• 1 year of previous hands-on clinical operations related experience

What else we look for (Preferred):

• Good computer skills in usage of MS Office Suite including Excel required
  Good written and verbal communication skills and interpersonal relationship skills
• Good problem-solving and critical thinking skills
  Good understanding and knowledge of fundamental principles, theories, and concepts relevant to clinical trial management
• Good problem-solving, organizational, analytical and critical thinking skills
  Strict attention to detail
• Ability to interact professionally with all organizational levels
  Ability to manage competing priorities in a fast paced environment
• Must be able to work in a team environment, including immediate supervisor and other team members in the section or group
  Ability to build productive internal/external working relationships
• Adhere to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control

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.

For California, the base pay range for this position is $56,000 to $80,000(highly experienced).

The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience).   Applications will accepted while this position is posted on our Career website.

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

COVID Vaccination Requirement

Edwards is committed to complying with the requirements and guidance from our government authorities and to protecting our vulnerable patients and the healthcare providers who