Global Feasibility Lead Ii

hace 6 días

Costa Rica Labcorp A tiempo completo

**Job Overview**:
Are you ready to redefine what’s possible, and discover your extraordinary potential at LabCorp? A career here provides the unique chance to create a lasting impact and difference in our patient’s lives. Joining our team will offer you a rewarding career, an opportunity to work in a high-energy & collaborative workplace, along with access to comprehensive benefits. Your work will be meaningful, the patient outcomes are real, and the results are lasting. With the support of exceptional people from across the globe and an energized purpose, you’ll be empowered to own your career journey with mentoring, training and personalized development planning.

Our mission is to help our clients bring the miracles of medicine to market sooner - join us for your next career move.

Responsibilities / 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 feasibility
- 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**:
- 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
- Minimum 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
**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**:

- 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
- 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
- Ability to inspire, to lead by example and motivate and negotiate with teams to seek solutions and get results
- Dem

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