Edwards Lifesciences Corp

Specialist, Clinical Development

Edwards Lifesciences Corp$87K — $123K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's Degree in biological or life sciences field
  • 3 years of experience in Class II and III medical device technologies or clinical studies
  • Proficiency in MS Office Suite and Adobe
  • Experience with documentation management systems (e.g., Ignite)
  • Excellent written and verbal communication skills
  • Demonstrated problem-solving and critical thinking abilities

Responsibilities

  • Ensure product development integrates essential clinical input for patient and physician benefits
  • Develop and implement pre-clinical test strategies and guide team execution
  • Design and conduct first-in-man product evaluations with appropriate case support
  • Create Clinical Investigator Brochure to support clinical trials
  • Provide scientific rationale for product attributes to obtain necessary approvals
  • Deliver product expertise for new product introduction training
  • Assess post-market evaluation results and conduct literature reviews

Benefits

  • Competitive salaries and performance-based incentives
  • Wide variety of benefits programs tailored to employee needs
  • Opportunities for professional development
  • Support for maintaining a healthy work-life balance
  • A safe workplace environment with adherence to health and safety protocols
Full Job Description
How you'll make an impact:
  • Ensures product development includes all necessary clinical input and aspects for the best interest of patients and utility for treating physicians.
  • Ensure successful product lifecycle management for multiple projects, including:
  • Develop and implement pre-clinical test strategy and provide guidance to team members on strategy execution
  • Design, prepare and conduct first-in-man product evaluations, including case support for proper product use
  • Create Clinical Investigator Brochure
  • Provide scientific rationale for product attributes and pre-clinical test results to regional clinical teams necessary to obtain site and country approvals
  • Provide product expertise for new product introduction training for clinical and site personnel
  • Design, develop, conduct, and assess results of post-market evaluations
  • Develop, review, and update clinical design control documents including technical summaries, clinical risk assessments, design of validation protocols and reports, design and application of FMEAs (Failure Modes and Effects Analysis), for technical and clinical documentation in moderately complex product development.
    Ensure medical and scientific factors are considered during cross-functional product development project team meetings.
    Design, review and/or conduct literature searches and complete literature reviews for design concept, product development, protocol preparation, clinical risk assessments and/or clinical evaluation reports.
    Evaluate collected data documentation and imaging media, draw findings, and make recommendations to complete product evaluations, product complaint review and other required interim or final reports.
  • Consult with field trial managers to gather field device performance feedback, as well as to ensure national and country clinical/regulatory requirements compliance.


What you'll need (required):
  • Bachelor's Degree in biological or Lifesciences field
  • 3 years previous related experience in Class II and III medical device technologies and/or clinical studies background


What else we look for (preferred):
  • Bachelor's Degree in engineering
  • Proven expertise in MS Office Suite, Adobe, and ability to operate general office machinery
  • Experience with documentation management systems (e.g., Ignite)
  • Excellent written and verbal communication skills and interpersonal relationship skills
  • Demonstrated problem-solving and critical thinking skills
  • Moderate knowledge and understanding of Edwards policies, procedures, and international and domestic medical device regulatory guidelines relevant to clinical studies
  • Moderate understanding of pre-clinical testing protocols, hospital environments and sterile techniques
  • Moderate knowledge of US and international medical device regulations, of Good Laboratory Practice (GLP) and Good Clinical Practice (GCP)
  • Ability to manage confidential information with discretion
  • Strict attention to detail
  • Ability to interact professionally with all organizational levels
  • Ability to manage competing priorities in a fast paced environment
  • Ability 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
  • 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 (CA), the base pay range for this position is $87,000 to $123,000 (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.

About Edwards Lifesciences Corp

Edwards Lifesciences is an American medical technology company headquartered in Irvine, California, specializing in artificial heart valves and hemodynamic monitoring. It developed the SAPIEN transcatheter aortic heart valve made of cow tissue within a balloon-expandable, cobalt-chromium frame, deployed via catheter. The company has manufacturing facilities at the Irvine headquarters, as well as in Draper, Utah; Costa Rica; the Dominican Republic; Puerto Rico; and Singapore; and is building a new facility due to be completed in 2021 in Limerick, Ireland.
Learn more about Edwards Lifesciences Corp
Size
15,700 employees
Market Cap
$45.6 billion
Industry
Net Income
$823.4 million
Founded
1958
5 Year Trend
+12%
Revenue
$4.3 billion
NASDAQ

Similar Jobs

More Jobs at Edwards Lifesciences Corp

More Pharmaceuticals & Biotech Jobs

Find similar Specialist, Clinical Development jobs: