Remote Global Feasibility Lead - Raleigh - job 853846

Covance

Date: 06/11/2021

City: Raleigh, North Carolina

Employment type: Full-time

Job Overview:


Do you have a passion for data and analytics? Are you interested in clinical trial planning with a focus on data driven decision making? Are you interested in combining real world data insights with factual clinical trial outcomes with an eye on the future of medicine? Then consider a role in the global feasibility team at Covance (soon to be labcorp drug development). We sit in the 'goldilocks zone' of trial planning, design, and execution where we are focused on bringing innovative data driven insights to our clients.


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 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 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 inter-departmental meetings, leading/contributing to the presentation of 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.


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


Contributes to best practice for feasibility conduct


Mentors junior team members (GFL1 or newer GFL2s as needed)


Performs any other duties as assigned


Education/Qualifications:


Minimum Required:


Qualified candidate has a Bachelor'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:


Masters degree in science-related discipline preferred


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





How to apply:

To apply for this job you have to sign in to our website (My profile link in the header).

If you don't have an account with us yet, please Sign up.