Site ID & Feasibility Specialist
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
1-2 years clinical research experience on Feasibility and/or Site Identification ready to enroll activities. Equivalent combination of education, training and experience.
Join IQVIA and let’s create a healthier world together:
Exposure across 21 Therapeutic Areas
Be part of a global team who operate across 141 locations
Exposure across a variety of studies and projects
Access to new, innovative technologies
Work within a collaborative and vibrant environment
Own your career!
Unleash your potential!
It takes passion to make the extraordinary possible for patients. Our culture of innovation and collaboration enables us to explore new possibilities and help improve health around the world.
When you join our diverse, global team, you’ll harness the power of unparalleled data, advanced analytics, cutting-edge technologies, and deep healthcare and scientific expertise to drive healthcare forward.
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.