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Job Requirements of Strategic Feasibility Lead:
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Employment Type:
Contractor
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Location:
Raleigh, NC (Onsite)
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Strategic Feasibility Lead
Careers Integrated Resources Inc
Raleigh, NC (Onsite)
Contractor
Job Title: Strategic Feasibility Lead
Job Location: Raleigh, NC- Hybrid (Preferably onsite hybrid Tues & Thurs Raleigh office)
Job Duration: 12 months +
Job Summary:
Job Location: Raleigh, NC- Hybrid (Preferably onsite hybrid Tues & Thurs Raleigh office)
Job Duration: 12 months +
Job Summary:
- Strategic Feasibility is a critical component in the execution of a clinical trial.
- The Strategic Feasibility Lead is a part of Program Delivery team with CLIENT’s Global Clinical Sciences & Operations (GSCO).
- This position is responsible to conduct, execute and oversee Feasibility work in collaboration with Contract Research Organizations (CRO)s to support CLIENT’s clinical development portfolio ranging from phase 1 to phase 4.
- Utilize and synthesize various internal and external data into meaningful feasibility solutions to support CLIENT’s clinical programs and studies.
- Support program/study level clinical planning; ensure accurate recruitment forecasting to maximize efficient and timely delivery of CLIENT’s clinical trials.
- Oversee and execute feasibility tasks in collaboration with CRO feasibility team and internal stakeholders, from early engagement throughout country and site selection.
- Coordinate and build consensus around program/study level planning and support stakeholders’ ad-hoc inquiries.
- Support group efforts to identify leading performance measures, enhance country and site selection strategies, and assist in the development of in-house feasibility tools.
- Ensure industry best practices and high-quality deliverables consistent with all applicable guidelines and regulations.
- Identify business improvement opportunities that improve overall GCSO’s Program Delivery, Site Engagement and Clinical Study Participant Experience & Recruitment capabilities with the guidance of the Head of Strategic Feasibility.
- A minimum of 5 years of experience in the Pharmaceutical, Biotechnology, and/or CRO industry is required with a preference towards individuals who have experience in clinical planning and/or clinical project management.
- Proven track record of working on cross-functional projects in a global environment.
- Previous project, team, or initiative leadership experience is preferred.
- Good working knowledge of GCP guidelines in different regions.
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