Clinical Records Representative

Imagine how your ideas and expertise can change a patients life. We generate extensive clinicalevidence to demonstrate the effectiveness and safety of our innovations and how our productstransform patients lives. As part of our Clinical Affairs team youll hone your scientific curiosity andpassion for evaluating data to increase access to pioneering technologies for patients in closepartnership with principal investigators dedicated medical professionals patient advocacy groups andregulatory authorities you will drive the evidence needed to optimize patient outcomes.

Patients with mitral and tricuspid heart valve disease often have complex conditions with limitedtreatment options. Our Transcatheter Mitral and Tricuspid Therapies (TMTT) business unit is boldlypursuing an innovative portfolio of technologies to address a patients unmet clinical needs. Its ourdriving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey.

As the Clinical Records Representative you will play a key role in ensuring the accuracy completeness and proper management of documentation that supports our clinical studies.

This is a hybrid position combining remote work with onsite collaboration. The selected candidate must live within a reasonable commuting distance of our Irvine Corporate location and be available for required onsite days.

How you will make an impact:

• Review and ensure accuracy and completeness of clinical study documents (e.g. EFS pivotal) ensuring GDP and performing quality checks with limited supervision.

• 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.

• Review clinical data for completeness of study files.

• May retrieve documents in support of internal and external audits utilizing knowledge of eTMF filing structure.

• Other incidental duties may include collating new study materials create study binders and patient recruitment materials and coordinating the shipment of materials to clinical sites.

What youll need (Required):

• H.S. Diploma or equivalent

• 2 years of previous related work experience

What else we look for (Preferred):

• Bachelors Degree in related field.

• Experience in preparing and managing regulatory documentation for clinical studies ensuring compliance with applicable guidelines and protocols.

• Good computer skills including MS Office Suite Adobe and ability to operate general office machinery.

• Experience with TMF.

• Good written and verbal communication skills and interpersonal relationship skills.

• Good knowledge and understanding of Edwards policies SOPs and domestic medical device regulatory guidelines relevant to clinical study documentation.

• Good knowledge of EW GDP (Good Document Practice) SOP requirements.

• Strict attention to detail.

• Ability to manage confidential information with discretion.

• Ability to manage competing priorities in a fast-paced environment.

• Ability to interact professionally with all team organizational levels.

• Must be able to work in a team environment under minimal supervision.

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 (CA)the base pay range for this position is $53000 to $70000 (highly experienced).

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

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

COVID Vaccination Requirement

Edwards is committed to protecting our vulnerable patients and the healthcare providers who are treating them. As such all patient-facing and in-hospital positions require COVID-19 vaccination. If hired into a covered role as a condition of employment you will be required to submit proof that you have been vaccinated for COVID-19 unless you request and are granted a medical or religious accommodation for exemption from the vaccination requirement. This vaccination requirement does not apply in locations where it is prohibited by law to impose vaccination.