Feasibility Specialist – Sponsor Dedicated

This is a fully remote position, open to applicants in Turkey.

📋 Description

• Assisting the Feasibility Lead to ensure understanding of the objectives, scope, and requirements of a Site Feasibility project, while guaranteeing the delivery of high-quality insights.

• Manage and maintain clinical trial management systems (CTMS) along with other relevant Feasibility tools.

• Conduct research and data analysis to pinpoint appropriate clinical trial sites.

• Support the setup of feasibility studies, which includes outreach to potential sites.

• Serve as a supportive team member for Regional Intelligence initiatives.

• Execute tasks across multiple Site Intelligence and Feasibility projects.

• Capable of handling a significant volume of studies and sites.

• Operate under the close supervision of the Regional Intelligence Team Lead, and, when necessary, the Feasibility Specialist Point of Contact (POC) or more experienced colleagues.

• Contribute to the execution of Site Feasibility plans and present findings to colleagues.

• Apply skills and discipline knowledge to Regional Intelligence development projects once proficiency in the role has been achieved.

• Foster a culture of continuous improvement to enhance processes for optimal efficiency and productivity.

• Develop and uphold internal processes aimed at optimizing country and site selection activities.

• Raise awareness by acting as a cross-functional team leader to deliver data, analytics, and regional site intelligence initiatives to a wide range of stakeholders, both internal and external.

• Oversee the operational and technical aspects of large global projects and assist with other Company systems activities related to site intelligence.

• Maintain effective relationships with various platform lines, Business Units/Research Units, and enabling lines to ensure successful portfolio delivery.

• Collaborate with broader clinical operations teams to enhance overall study start-up metrics and implement streamlined processes.

⛳️ Requirements

• Minimum of 2 years of relevant experience.

• Multilingual: Fluent spoken and written proficiency in the local language alongside English.

• Strong verbal and written communication skills for effective interaction with colleagues and stakeholders both internally and externally.

• Excellent presentation abilities, interpersonal skills, and a collaborative team-oriented mindset.

• Outstanding verbal, written, communication, and time management capabilities.

• Capacity to multitask under tight deadlines across several projects with specific and unique requirements, while maintaining attention to detail and delivering high-quality work.

• Experience within a clinical research organization and relevant therapeutic specialties, with familiarity in principles, concepts, practices, and standards.

• Background in the pharmaceutical industry or CRO, or experience at a site in a similar capacity.

• Previous feasibility experience is preferred.

🏝️ Benefits

• • •