Global Feasibility Lead Ii

2 meses atrás

São Paulo SP, Brasil Fortrea Tempo inteiro

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.

Job Summary:

- The Global Feasibility Lead 2 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 2 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 2 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._
- The Global Feasibility Lead 2 role requires a diverse skill set; strong data mining and analytics skills, writing and presentation skills, and customer management skills are required. Comfort with participating in and/or leading client facing interactions as it relates to presenting feasibility related findings and recommendations is necessary._

Essential Job Duties:

- 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

F. Travel Requirements:
% of time_: 10-15%_

% of the above that requires overnight stay: 80%

Travel will likely be mínimal; however from time to time there will be a need to attend
- conferences, client meetings, vendor meetings
- International and Domestic travel maybe required, including air travel & overnight stays
- Ability and willingness to present at internal and external meetings

II. Experience:
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.

Preferred:

- Master degree in science-related discipline
- Understanding of therapeutic drug or device development and marketing
- Minimum of 4 years 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
- At least 2 years of 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
- A

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