Edwards Lifesciences Corp

Senior Manager, Clinical Safety

Edwards Lifesciences Corp$139K — $196K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in a related field.
  • 5-7 years of relevant experience in clinical safety or equivalent.
  • Proven experience in people management or equivalent.
  • Preferred: Master's degree in a related field.
  • Experience in the medical device or pharmaceutical industry.
  • Experience in regulated environments.

Responsibilities

  • Oversee and mentor clinical safety team to achieve results.
  • Develop and align safety processes, including SOPs and charters.
  • Act as a liaison for safety matters among cross-functional teams.
  • Provide input on clinical trial design and regulatory submissions.
  • Represent safety during audits.

Benefits

  • Competitive salaries and performance-based incentives.
  • Diverse benefits programs to meet individual needs.
  • On-site opportunities at the corporate headquarters in Irvine, CA.
Full Job Description
The Senior Manager, Clinical Safety will manage a team of clinical research professionals providing oversight, mentoring and guidance to drive results in support of safety related activities within the Transcatheter Heart Valve business unit.

This role requires onsite presence at our corporate headquarters in Irvine, CA.

You will make an impact by:
  • Manage and oversee the work of the clinical safety team, providing oversight and guidance cross functional or matrix teams as appropriate. Develop a robust talent development plan in alignment with functional growth strategies of the department
  • Develop and ensure alignment of safety processes (e.g., safety work instructions and documents, SOPs, charters) as needed. Identify risk, develop and lead in the implementation of clinical safety strategies which may include negotiations with internal and external parties
  • Act as a liaison to key cross-functional stakeholders (e.g., PMO, Clinical Affairs, Regulatory Affairs, Quality, study sites leadership) regarding Safety-related matters
  • Provide input on clinical trial design and safety sections of study protocols, CRFs, regulatory submissions, and clinical/regulatory reports and provide input to regulatory affairs questions on safety related issues
  • Represent safety in internal and external audits


What you'll need (Required):
  • Bachelor's Degree in in related field, with 5-7 years previous related experience or equivalent work experience based on Edwards criteria
  • Demonstrated track record in people management or equivalent work experience based on Edwards criteria


What else we look for (Preferred):
  • Master's Degree or equivalent in related field
  • Experience in Medical device or pharmaceutical industry, Clinical research, or in-hospital clinical and/or managerial experience or equivalent work experience based on Edwards criteria
  • Experience working in a regulated industry or equivalent work experience based on Edwards criteria
  • Demonstrated ability to manage assigned team and provide coaching and feedback, including responsibility for all employee actions including hire/fire authority and partnering with HR on all aspects of employee relations
  • Excellent problem-solving, organizational, analytical and critical thinking skills including high discretion/judgment in decision making
  • Excellent written and verbal communication skills and interpersonal relationship skills including negotiating and relationship management skills with ability to drive achievement of objectives
  • Good understanding of related aspects of clinical studies processes and/or systems
  • Ability to develop and integrate metrics into the projects and operations that clearly demonstrate the value to the business


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 $139,000 to $196,000 (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

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