Feasibility Specialist - Sponsor Dedicated - Home based

Parexel FSP is looking to hire a Feasibility/site  for one of our key sponsors.

This role is responsible for Supporting the Feasibility Lead to ensure knowledge of the goals, scope and requirements of a Site Feasibility project, and ensures that high-quality insights are delivered.

You’ll administer and maintain clinical trial management systems (CTMS) and other relevant Feasibility tools. Whilst performing research and data analysis to identify suitable clinical trial sites.

Also, you will assist with the setup of feasibility studies, including outreach to potential sites.

• Acts as a supportive team member for Regional Intelligence
• Performs tasks for multiple Site Intelligence and Feasibility projects.
• Able to manage multiple volume of studies and sites
• Works under close supervision of Regional Intelligence Team Lead, and where needed the Feasibility Specialist Point of Contact (POC) or more experienced colleagues
• Contributes to executing Site Feasibility plans and presenting the data to colleagues.
• Applies skills and discipline knowledge to Regional Intelligence development projects, when proficiency in role has been mastered
• Promotes a continuous improvement culture to streamline appropriate processes for maximum efficiency and productivity
• Develops and maintains internal processes aimed to optimize country & site selection activities
• Creates awareness by working as a cross functional team leader to deliver data, analytics and regional site intelligence initiatives across a broad spectrum of stakeholders, both internal and external
• Runs operational and technical aspects of large global projects and assists with other Company systems activities related to site intelligence
• Maintains effective relationships with other platform lines, Business Units/Research Units, and enabling lines that facilitates effective portfolio delivery
• Partners with wider clinical operations teams to improve overall study start up metrics and implement simple processes

• In general, candidates for this job would have the following levels of experience in Clinical Research/Clinical Operations: 2 years
• Multilingual:
  Fluent spoken and written abilities in local language in addition to English
• Effective verbal and written communication skills in relating to colleagues and stakeholders both inside and outside of the organization
• Strong presentation skills, interpersonal skills, as well as a team oriented approach. Excellent verbal, written, communication and time management skills
• Ability to multitask under tight deadlines on several projects with specific and unique requirements, while providing attention to detail and high quality work
• Experience in a clinical research organization and related therapeutic specialties with familiarity in principles, concepts, practices and standards.
• Experience working in the pharmaceutical industry or CRO or at site in a similar role
• Prior feasibility experience