In-house Clinical Research Specialist - Irvine, United States - Edwards Lifesciences

Edwards Lifesciences

Verified Company

Irvine, United States

1 week ago

Posted by:

Mark Lane

beBee recruiter

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.

As the Clinical Research Specialist, you will ensure clinical trials are conducted and reported in accordance with all applicable regulatory requirements.

You will make an impact by...
Performing study start-up and conduct activities including ICF review that meets regulatory requirements, creating study specific essential document lists, managing and communicating the status of study progress and activities
Conducting in-house and site (if applicable) reviews of associated documentation and participating in internal and competent authority (e.g., FDA, DEKRA, PMDA) audits to ensure all essential clinical Trial Master File (TMF) documents are compliant with Good Documentation Practices, Edwards internal SOPs, and US and OUS regulations
Assessing current processes, identify opportunities and propose solutions to improve process efficiency within and across related functional areas
Partnering with cross-functional team (e.g., clinical data management, field teams) with query management, data reviews and resolution
Other incidental duties

What you'll need (required):

Bachelor's Degree or Equivalent in Life Sciences or Nursing
3 year's experience in clinical research (site management, clinical project management, monitoring, and/or CRC) including quality assurance/control and regulatory compliance or field monitoring with experience in the healthcare industry

What else we look for (preferred):
Experience in electronic data capture
Covid Vaccination
Ability to travel nationwide up to 10% for site visits, and conferences
Good computer skills in usage of MS Office Suite and Clinical Systems such as CTMS (Clinical Trial Management System), eTMF (electronic Trial Master file) preferred
Strong written and verbal communication skills, presentation skills, interpersonal relationship skills, and analytical skills are required
Strong problem-solving and critical thinking skills
Strong understanding of cardiovascular anatomy, pathology and physiology or Business Unit area of expertise
Moderate understanding of regulatory submissions, reporting, and audits
Ability to manage confidential information with discretion
Ability to manage competing priorities in a fast paced environment
Must be able to work in a team environment, including inter-departmental teams and representing the organization on specific projects
Ability to build productive internal/external working relationships

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 $83,000 to $117,000(highly experienced).