Vacancy title:
Site ID Svcs Specialist 2
Jobs at:
IQVIADeadline of this Job:
30 September 2020
Summary
Date Posted: Thursday, September 24, 2020 , Base Salary: Not Disclosed
JOB DETAILS:
IQVIA, formerly Quintiles and IMS Health, Inc.,is an American multinational company serving the combined industries of health information technology and clinical research. It is a provider of biopharmaceutical development and commercial outsourcing services, focused primarily on Phase I-IV clinical trials and associated laboratory and analytical services, including consulting services. It has a network of more than 58,000 employees in more than 100 countries.As of 2017, IQVIA was reported to be one of the world's largest contract research organizations.
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 specifications of the protocol.
• Collect and analyze country/regional Feasibility and/or Site Identification information to meet timelines of each study.
• Attend kick off meetings to understand study requirements include investigator profile, protocol, process specifics and timelines.
• Raise questions and make suggestions based on SID SOPs and Work Instructions.
• Distribute, track, negotiate and review the Confidential 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 for 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.
Job Skills: Not Specified
Qualifications
• 3 years clinical research experience. Equivalent combination of education, training and experience
• At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 67,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way
Job Education Requirements: Not Specified
Job Education Experience: Not Specified
Work Hours: 8
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