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Senior Manager, Global Trial Optimization

ManagerManagerOtherRemoteSeniorTeam 10,001+Since 1988H1B SponsorCompany SiteLinkedIn

Location

United States

Posted

81 days ago

Salary

$134.4K - $219.2K / year

Seniority

Senior

Bachelor Degree8 yrs expEnglish

Job Description

Senior Manager, Global Trial Optimization

Regeneron

• Lead study level feasibility processes to generate high quality and timely data to inform study design, efficient geographical placement and operational planning. • Partner with teams during CRO led feasibility activities supporting validation of study and country level enrollment rates and study start up timelines to advise budget and baseline setting. • Supports the development and implementation of the Global Trial Optimization function through process initiatives and change management. • Partner with Data and Analytics function to review and identify appropriate central data sources. • Articulate the data story to teams based on country level feasibility and centrally derived data to support data driven decisions to improve protocol design • Project management of study level country landscape assessment activities and the collection of targeted feasibility information for early assessment of operational feasibility for conducting clinical trials. • Lead study level engagements to acquire, analyze and deliver high quality targeted information from external partners. • Prove input into continuous improvement activities to ensure consistency of process execution. • In partnership with Clinical Outsourcing provide functional input into the identification, qualification and relationship management of a range of vendors. • Develop and implement patient recruitment and retention tactics aligned with defined study strategy. • Develop and maintain knowledge of external clinical trial environment and assess developments for impact on study design and execution. • May require up to 20% travel

Job Requirements

  • Bachelor's degree in a related field
  • Minimum of 8 years of relevant industry experience within pharma/biotech, a CRO or consulting
  • Strong understanding and experience in operationalizing clinical development programs in a global setting from first-in-human to post-approval.
  • Experience with feasibility.
  • Must be a compelling communicator with ability to translate sophisticated messages to a variety of audiences.
  • Experience in using data to inform clinical strategy development
  • Ability to understand sophisticated business questions and develop effective solutions
  • Experience in process development, implementation and change management activities
  • Line management experience preferred

Benefits

  • health and wellness programs (including medical, dental, vision, life, and disability insurance)
  • fitness centers
  • 401(k) company match
  • family support benefits
  • equity awards
  • annual bonuses
  • paid time off
  • paid leaves (e.g., military and parental leave) for eligible employees at all levels!

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