Sr Site ID & Feasibility Specialist

IQVIA LLC; Fatih; On-site; TRY 110,000 - 170,000; Full time

Job summary

IQVIA LLC in Turkey is seeking a Sr Site ID & Feasibility Specialist to lead feasibility activities and site identification for regional studies, with hybrid work arrangements. You will manage opportunities, ensure adequate investigator networks, collect feasibility data, and coordinate site contracts and questionnaires while coordinating with study teams to meet timelines and sponsor requirements.

The role requires collaboration with sponsors, regulatory teams and cross-functional partners to

Qualifications

• Bachelor’s degree in Life Sciences, or related field.
• 3 years of clinical research experience on Feasibility and/or Site Identification.
• Strong problem solving, negotiation and communication skills.

Responsibilities

• Manage opportunities/projects/programs for country or region and meet timelines and budget.
• Ensure site list for assigned studies includes adequate investigators per protocol.
• Collect and analyze country/regional Feasibility and Site Identification data.
• Attend kickoff meetings to understand study requirements and timelines.
• Distribute, track, negotiate and review CDAs for Feasibility and Site Identification.
• Distribute and review Site Questionnaires and Site Qualification Questionnaires.
• Maintain investigator databases and ensure complete site information.

Skills

Problem solving

Negotiation

Communication

Multi-project management

Education

Bachelor’s degree in Life Sciences

Job description

Sr Site ID & Feasibility Specialist Turkey - Hybrid

Make an impact on patient health! IQVIA’s Global Site Activation Team of 2000 employees, drives best in class site and customer experience, with industry leading outcomes. We keep the patient at the forefront; ‘Always Impatient for the Patient’ and we excel in our collaboration with our external/internal customers. IQVIA’s Country Site Activation team are a global network who identify and activate sites to the highest quality to ensure patients on Clinical trials have access to safe and effective medication. We are leaders in innovation and first to new technologies, meaning a vast amount of career development opportunities are available.

Job Overview

Manage and lead activities associated with Feasibility and/or Site Identification for regional and/or country projects and/or programs.

Essential Functions

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.

Qualifications

Bachelor’s degree in Life Sciences, or a 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 functional/regulatory requirements, including local regulations, SOPs and ICH/GCP

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.

Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere.

Thank you for your interest in growing your career with us.