Edwards Lifesciences Corp

Senior Manager, Clinical Project Management, Global Clinical Research Aortic

Edwards Lifesciences Corp$139K — $196K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's Degree in a related field
  • 10+ years of relevant experience or equivalent work experience
  • Master's Degree or equivalent preferred
  • 8+ years of relevant experience preferred
  • Certification in a related discipline preferred
  • Proven project management skills
  • Expert knowledge in clinical systems such as CTMS and eTMF

Responsibilities

  • Manage clinical trial activities ensuring compliance with regulatory requirements
  • Synthesize large sets of clinical trial data for operational strategies
  • Develop and manage clinical project plans to meet trial milestones
  • Oversee clinical core teams in executing complex projects
  • Communicate project status and coordinate with internal and external stakeholders
  • Analyze trial performance and develop corrective actions as needed
  • Identify study risks and implement mitigation strategies

Benefits

  • Competitive salaries and performance-based incentives
  • Comprehensive benefits programs tailored to employee needs
  • Opportunity for professional mentoring and coaching
  • Engagement with executive and industry conferences
  • Work in a collaborative environment within a large reputable organization
Full Job Description
How you'll make an impact:
  • As the Manager of Clinical Project Management THV Global Clinical Research, you will manage clinical trials activities and ensure all applicable regulatory requirements are met.
  • This role requires the ability to synthesize large sets of clinical trial data to support innovative operational strategies.
  • Experience working with long-term clinical trials, IDE and Post approval, in a matrix organization, and ability to oversight clinical core team in navigating data cleaning process for regulatory submissions is essential.
  • Develop and manage clinical project plans to identify and complete clinical trial milestones with accountability for successful completion of all project deliverables in for larger or more complex clinical trials in accordance to GCP, all applicable regulations, and SOPs.
  • Serve as the primary lead of assigned clinical trial(s) Provide direction, guidance, and oversight of clinical core teams to execute larger or more complex projects and initiatives.
  • Determine clinical trial resources and set priorities for projects. Manage project status and appropriate communication both internally and externally. May present trial information at executive and/or industry conferences
  • Analyze trial performance to plan and develop corrective actions, gain alignment with leadership on proposals prior to implementation
  • Identify and communicate study risks, recommend and lead implementation of mitigation strategies in alignment with management
  • Oversee the selection and deliverable of clinical vendors and study sites
  • Provide mentoring and coaching to other project team members


What you'll need (Required):
  • Bachelor's Degree in related field, 10 years experience of previous related experience or equivalent work experience based on Edwards criteria


What else we look for (Preferred):
  • Master's Degree or equivalent in related field, 8 years experience of previous related experience or equivalent work experience based on Edwards criteria Preferred
  • Experience working in a large manufacturing company or equivalent work experience based on Edwards criteria Preferred
  • Other: Certification in related discipline Preferred
  • Proven successful project management skills
  • Proven expertise in usage of MS Office Suite and Clinical Systems such as CTMS (Clinical Trial Management System), eTMF (electronic Trial Master file) preferred
  • Excellent written and verbal communication skills and interpersonal relationship skills including negotiating and relationship management skills with ability to drive achievement of objectives
  • Recognized as an expert in own area with specialized depth within the organization
  • Expert knowledge and understanding of Edwards policies, procedures, and international and domestic medical device regulatory guidelines relevant to clinical protocols
  • Expert understanding of regulatory submissions, reporting, and audits
  • Ability to manage confidential information with discretion
  • Strict attention to detail
  • Ability to interact professionally with all organizational levels and proactively escalate issues to appropriate levels of management in the organization
  • Ability to manage competing priorities in a fast paced environment
  • Represents leadership on projects within a specific area interfacing with project managers and clinical team
  • Consult in project setting within specific area
  • Provides leadership to outsourcing partners on a task level, and may participate on small scale RFP
  • 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 $139,000 - $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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