Covance

Global Feasibility Lead

Company
Covance
Location
Hungary
Salary
Competitive
Posted
04 Mar 2021
Closes
08 Mar 2021
Ref
10024_59068-hungary
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

The Global Feasibility Lead position can be home or office based anywhere within the EMEA region.

  • Access to one of the largest clinical trial performance datasets in the industry
  • Conducting searches and analysis of internal and external data assets to develop data-driven recommendations for trial conduct
  • Engaging and supporting scientific, medical and operational teams globally


Role responsibilities:

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 clinical trials (country/site mix, site selection, enrolment modelling.).

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.

Actively participates on cross-functional teams that plan, analyze, and present proposals and bid defenses as part of winning new business and maintaining client base.

Serves as functional bidder for multiple service and stand-alone RFPs as appropriate; prepares/oversees preparation of the budget and text for proposals for which feasibility and/or site identification is included.

Leads cross functional teams to coordinate full feasibility efforts; responsible for final report creation and delivery, as well as presentation to the client in close collaboration with Covance therapeutic experts.

Participates in intra and inter-departmental meetings, presenting information on feasibility offerings, demonstrating continued value-add 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.

#LI-NC1 EMEA REMOTE

Education/Qualifications:
Minimum Required:
 Qualified candidate has an Associate's degree with equivalent work experience or equivalent years relevant work experience.
 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.
Preferred:
 Master degree in science-related discipline

Experience:
 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.
Preferred:
 Understanding of therapeutic drug or device development and marketing
 Experience working in an academic, science/health-related 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
 Relevant industry experience within pharma/biotech, a CRO or consulting firm (or equivalent) is desired

Position-specific Requirements:
 Strong data mining and analytical skills
 Strong writing and presentation skills
 Upholds the highest standard of personal professionalism and work integrity
 Demonstrated ability to work independently
 Strong attention to detail/quality control 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
 Ability to establish and maintain effective working relationships with team members, management, operations staff, clients, and executive management
 Demonstrated ability to handle multiple competing priorities effectively
 Negotiation and relationship management skills
 Experience in analysing study and investigator performance metrics
 Self-motivated, works effectively under pressure

Technical Requirements:
 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
 Strong skills in scientific data manipulation, analysis, reporting and maintenance
 Proven written and verbal communication skills, with strengths in independently gathering/presenting data in support of operational strategy and planning