Feasibility Specialist – Sponsor Dedicated
Location
Turkey
Posted
1 day ago
Salary
0
Seniority
Mid Level
Job Description
Feasibility Specialist – Sponsor Dedicated
Parexel
• 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. • Administer and maintain clinical trial management systems (CTMS) and other relevant Feasibility tools. • Perform research and data analysis to identify suitable clinical trial sites. • 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.
Job Requirements
- 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.
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