Global Feasibility Lead

1 semana atrás

Oeiras, Lisboa, Portugal Labcorp Tempo inteiro

As a leading contract research organization (CRO), Labcorp Drug Development (formerly known as Covance) provides comprehensive drug development solutions for a range of industries.

Our services cover the preclinical, clinical and post-market phases of drug development, the product life cycles for medical device and diagnostics and development services paired with regulatory support for the chemical testing and crop protection industries.

Labcorp Drug Development is a global leader in nonclinical safety assessment, clinical trial testing and clinical trial management services. Our unique perspectives are based on decades of scientific, medical and regulatory expertise.


Our positions offer excellent exposure to a range of disease areas, and a real opportunity for career progression and promotion in time.


Role Details:


We are recruiting for our
multi-sponsor business and are currently seeking to hire a
Global Feasibility Lead with a
permanent and
full-time contract.

This is a fully
remote/home-based position.

Responsibilities:


The Global Feasibility Lead will play an integral role in operational strategy and planning in the pre-award space through participation in strategy development conversations, robust primary and secondary data collection and analysis, and development of feasibility and site selection strategies.


In addition, the Global Feasibility Lead will be responsible for managing global feasibility projects, working closely with representatives within the company to deliver robust feasibility reports to our customers.

The Global Feasibility Lead will transition the site selection strategy to operations in the post-award space by handing over relevant pre-award findings to the site selection team.


  • Accountable for supporting the development, analyses, interpretation and presentation of primary and secondary data in support of operational strategy and planning
  • Conducts data mining of internal and external databases and initiates/oversees the collection of primary data for use in development of robust strategies for global clinical trials (country/site mix, site selection, enrollment modeling)
  • Participates in the development of proposals and bid defenses; provides recommendations on the most appropriate use of data to support proposals and bid defense presentations, works with the team to identify potential risks, and is learning to propose effective solutions as appropriate
  • Actively participates on crossfunctional teams that plan, analyze, and present proposals and bid defenses as part of winning new business and maintaining client base
  • Serves as functional bidder reviewer of the budget and text for proposals for which feasibility and/or site identification is included as the primary deliverable
  • Leads cross functional teams in standalone feasibility efforts; responsible for final report creation and delivery, including discussion of findings and recommendations with external clients
  • Participates in intra and interdepartmental meetings, leading/contributing to the presentation of information on feasibility offerings, demonstrating continued valueadd of the department and providing training on best practices, processes and tools
  • Develops networking abilities and has an ability/willingness to work with individuals across the globe
  • Leads and/or contributes to process improvement or special projects within FSS
  • Lead and/or contributes to development, implementation, and maintenance of systems within FSS

Requirements:

  • Bachelor's degree with equivalent work experience or equivalent years relevant work experience at minimum
  • Practical experience and understanding of global drug development and clinical trials including demonstrated experience for the mining, manipulating and presenting of complex scientific data as it relates to clinical research and market analyses
  • Strong data mining and analytical skills
  • Strong writing and presentation skills
  • Ability to successfully and quickly understand scientific information so as to be able to independently source data/information relevant to a scientific/medical strategy
  • Demonstrated ability to handle multiple competing priorities effectively
  • Negotiation and relationship management skills
  • Experience in analyzing study and investigator performance metrics
  • Excellent computer skills, including strong working knowledge of Microsoft Office and other data capture and compilation tools
  • Established knowledge of tools used in obtaining critical market analyses of therapeutic pipelines
  • Minimum 4 years working in an academic, science/healthrelated industry, or consulting field with responsibilities for the mining, obtaining (across disparate sources), manipulating and presenting of complex scientific data as it relates to clinical research is preferred
  • At least 2 years of relevant industry experience within pharma/biotech, a CRO or consulting firm (or equivalent) is desired
**Labcorp is proud to

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