Global Feasibility Lead
- Employer
- Labcorp
- Location
- Belgium
- Salary
- Competitive
- Start date
- 3 Mar 2021
- Closing date
- 8 Mar 2021
View more
- Discipline
- Clinical Research, Study Start Up
- Hours
- Full Time
- Contract Type
- Permanent
- Experience Level
- Experienced (non-manager)
Job Details
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
Company
At Labcorp, we believe in the power of science to change lives. We are a leading global life sciences company that delivers answers for crucial health questions —because we know that knowledge has the potential to make life better for all. Through our unparalleled diagnostics and drug development capabilities, we provide insights and accelerate innovations that not only empower patients and providers but help medical, biotech, and pharmaceutical companies transform ideas into innovations. Here, you can join our more than 70,000 employees, serving clients in more than 100 countries, as we work together to make a real impact on people’s lives. Join us in our pursuit of answers.
- Website
- https://careers.labcorp.com/global/en
- Location
-
Maidenhead Office Park
Westacott Way
Littlewick Green
Maidenhead
SL6 3QH
United Kingdom
Get job alerts
Create a job alert and receive personalised job recommendations straight to your inbox.
Create alert