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Associate Director, Global Feasibility

4 months ago

Hanover, United States CSL Full time

Joining CSL as Associate Director Global Feasibility offers an exciting opportunity to be part of a continually growing team dedicated to the end-to-end feasibility and study start up delivery. The role is made for a dynamic candidate with outstanding analytical skills and an easy way to communicate the data in a recommended feasibility strategy to stakeholders and governance. Do you have a track record of using diverse datasets for purposes of analysis and intelligence to drive assessments? -Please, have a look at the below: This role may be for you

Want to make an application Make sure your CV is up to date, then read the following job specs carefully before applying.

The Associate Director, Global Feasibility, is the strategic interface with Clinical Development and Clinical Portfolio Execution to provide quality-by-design/strategic insight on protocol and country early feasibility and build allocation strategy scenarios in line with budget. The role is also the primary interface with the Global Medical Affairs and Commercial Development organizations to ensure country input into the country strategy and works closely with other functional area leads to ensure global consistency.

The role will provide leadership to the feasibility and start-up team across all clinical programs in accordance with the company strategy, timelines, budget and quality expectations.

This role will collaborate closely with the site management team and site partnership to build a strong global site network and collaborate with the external service providers and site management group to develop a feasibility, start-up and study enrolment strategy with appropriate mitigation to meet the study and program target within timeline.

Main Responsibilities and Accountabilities

  • Accountable for the development of the feasibility strategy across clinical programs and delivering its end to end process.
  • Lead and manage the global feasibility and collaborate with internal functional area leads (e.g. Regulatory Affairs, Clinical Vaccine Group) to build knowledge on study and country interest and feasibility and help to respond to the external environment.
  • Pro-actively improve cross-business collaboration and leverage site relationships, data analytics and internal cross-functional knowledge/ expertise to build intelligence.
  • Leverage historical, scientific, epidemiologic and competitive data to identify and evaluate new regions/countries in line with the company strategy and in collaboration with Global Medical Affairs and Commercial group.
  • Collaborate with the Program Director/ Clinical Science & Strategy and Global Clinical Program Manager to provide analyses and data for scenario planning and country strategy, including region/country identification and evaluation.
  • Ensure effective collaboration with external service providers to further build feasibility and country strategy for a given study including mitigations for enrolment.
  • Ensure oversight of the enrolment strategy and mitigations until the study has completed enrolment
  • Ownership of the Feasibility Mobilization process. Establish, implement and manage standards and processes for initiating study planning and feasibility activities, including build of data driven study assumptions from protocol go through feasibility completion.
  • Full support of the feasibility process. Maintain continuity across studies by documenting changes from Early Estimates, Early Feasibility, Detailed Assumptions, Detailed Feasibility, to Recruitment & Start Up Planning.
  • Partner with Clinical Operations management to implement processes and work practices that drive rapid, accurate and robust assessments of program and protocol feasibility at both the country and site level, as well as the timing of key recruitment milestones. Involve relevant stakeholders in the feasibility process to ensure all needs are considered and realistic study enrolment plans are developed and in place. Review and Implement tools or systems to streamline the feasibility process with stakeholders.
  • Upholds and promotes the Company's reputation externally by demonstrating high professional standards and integrity in all external contacts.
  • Maintains up to date knowledge of the Study Operations landscape, industry best practices and regulatory considerations.

Background education and past experience

  • BS/BA degree required - Graduate degree desirable in a relevant field such as Operations, analysis, healthcare, MBA
  • 10+ years of Clinical Operations experience, including detailed assessment/analysis and reporting of program operational plans and options
  • Experience in overseeing complex and multi regional Global Clinical Trials
  • Track records of strategically advising leaders on operational environment and best ways to succeed in plan execution.
  • Track record of using diverse datasets for purposes of analysis and intelligence
  • Demonstrated proficiency in advanced MS Project, Microsoft Word, PowerBI
  • Experience in overseeing complex and multi-regional Global Clinical Trials
Our Benefits

We encourage you to make your well-being a priority. It's important and so are you. Learn more about how we care at CSL.

About CSL Behring

CSL Behring is a global leader in developing and delivering high-quality medicines that treat people with rare and serious diseases. Our treatments offer promise for people in more than 100 countries living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. Learn more about CSL Behring.

We want CSL to reflect the world around us

As a global organisation with employees in 35+ countries, CSL embraces diversity and inclusion. Learn more about Diversity & Inclusion at CSL.

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