Senior Feasibility & Site Identification Lead

IQVIA; Fatih; Hybrid; TRY 250,000 - 340,000; Full time

Job summary

IQVIA’s Global Site Activation Team in Turkey is seeking a Sr Site ID & Feasibility Specialist to lead feasibility and site identification for regional studies, ensuring investigators meet protocol needs and timelines. You will manage opportunities within budgets, coordinate CDAs and site questionnaires with study teams and Legal, and maintain investigator databases and country information repositories.

This hybrid role requires strong problem solving, negotiation, and regulatory knowledge to

Qualifications

• Bachelor’s degree in Life Sciences or related field.
• 3 years clinical research experience on Feasibility and/or Site Identification ready to enroll activities.
• Strong problem solving skills.
• Ability to negotiate and have strong communication skills.
• Ability to work on multiple projects.
• Knowledge of applicable regulatory requirements, including local regulations, SOPs and ICH/GCP.

Responsibilities

• Manage assigned opportunities/projects/programs for country or region and adhere to timelines and budget.
• Ensure the site list for assigned studies includes an adequate number of appropriate investigators in accordance with the needs of the sponsor and specificataions of the protocol.
• Collect and analyze country/regional Feasibility and/or Site Identification information to meet timelines of each study.
• Attend kick off meetigs to understand study requirements include investigator profile, protocol, process speoifics and timelines.
• Raise questions and make suggestions based on SID SOPs and Work Instructions.
• Distribute, track, negotiate and review the Condidential Disclosure Agreements (CDAs) for Feasibility and/or Site Identification with input from the study team, management and Legal when appropriate.
• Distribute, track and review Site Questionnaires for Feasibility and/or Site Information Forms or Site Qualification Questionnaires for SID
• Ensure completeness, site capability and suitability fo the study.
• For SID review SIF and/or SQQ vs the guidance document and approve for SSV or select appropriate sites.
• Manage investigator database entry and quality, ensuring complete investigator and site information is captured and monitor for duplicate entries.
• Maintain and update company information repositories and databases.

Skills

Problem solving

Negotiation

Communication

Multitasking

Regulatory knowledge

Education

Bachelor’s degree in Life Sciences or related field

Job description

IQVIA’s Global Site Activation Team in Turkey is seeking a Sr Site ID & Feasibility Specialist to lead feasibility and site identification for regional studies, ensuring investigators meet protocol needs and timelines. You will manage opportunities within budgets, coordinate CDAs and site questionnaires with study teams and Legal, and maintain investigator databases and country information repositories.

This hybrid role requires strong problem solving, negotiation, and regulatory knowledge to