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VP, Head Clinical Trial Management - Oklahoma City, United States - Scienta
Description
Location:
East Coast, US
This role is only open to candidates that already have the right to work in the US. No sponsorship available.
The Company
We are partnered with a leading global biopharma company that is transforming the lives of patients with rare disease through a novel class of medicines.
Having delivered the world's first and only approved treatment in this area of therapeutics, they are continuing to advance their pipeline across several other therapeutic areas.
The RoleThe Head of Clinical Trial Management will be part of the Clinical Operations Leadership Team at the level of Vice President.
This role will be the SME and accountable for the delivery of studies within the assigned portfolio, to provide the strategy input and clinical operations expertise that will inform overall program strategy.
Whilst leading a team of 20 study managers, this position will look to optimize global clinical study delivery.Main Responsibilities
Manage a diverse portfolio of assets across different therapeutic areas, ensuring the effective and efficient delivery or high-quality clinical trials
Act as the primary liaison for clinical operation leads furnishing critical content for governance meetings, regulatory submissions and investment planning
Accountable for optimised clinical trial delivery plans, representing clinical operations at forums and key alliance partnerships
Facilitate the identification of suitable clinical trial sites and engage with stakeholders to enhance site relationship management
Collaborate with Global Trial Optimization and CROs to furnish precise, data-driven study time-lines, milestones, enrolment projections, and cost estimates
Supervise clinical trial budgets and operations, including resource allocation, priority setting, and operational planning
Steer the formulation and execution of Study Management standardizations, encouraging adaptability for swift execution and inventive solutions.
Requirements
Masters or PhD education
15+ years experience in drug development (start-up to final study report)
5+ years line management experience in Clinical Trials
Advanced financial knowledge (E.g. resource planning, forecasting, and budgeting)
Extensive industry network in Clinical Operations
Flexibility to travel
How to Apply
Apply here for a confidential call about this opportunity.
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