Pfizer - SIS US

Parexel International Corporation

Multiple Locations

US - REMOTE - ANY LOACTION******

Site Intelligence Specialist (SIS)

Position Purpose: The Site Intelligence Specialist (SIS) acts as a supportive team member for Site Intelligence and Site Selection.The SIS performs tasks for multiple Site Intelligence and Feasibility projects.The SIS contributes to executing Site Feasibility plans and presenting the data to colleagues.

Organizational Relationships: Reports to ExecuPharm/Parexel FSP-assigned Line Management with day-to-day direction from Client. Refer to Organizational Chart for details regarding assigned role and associated reporting structure.Works under close supervision of Director of Site IntelligenceCollaborates across functional lines within Clinical Development and Operations (CD&O) and Worldwide Research, Development & Medical (WRDM), Contract Research Organizations (CROs), Functional Service Providers (FSPs).

Primary Responsibilities: Supports the Site Intelligence Lead to ensure knowledge of the goals, scope and requirements of the Site Feasibility project and ensure that high quality results are delivered.Participates in the Site Intelligence by reviewing internal and external intelligence on performance and quality metrics and performing literature research to identify investigators to build the database. Collects information supporting the definition of the ideal site for a study.Upon request from Site Intelligence Lead provides country specific data (site contact, site recommendations) generated through collecting and interpreting feasibility data.Interacts with internal and external personnel to coordinate the collection of site feasibility data and contributes to the development and maintenance of the Investigator/Site Networks database to build a comprehensive list of investigational sites across all therapeutic areas per country.Maintains, verifies, processes, and makes updates to Client systems (including Registry), spreadsheets/documents as needed.Promotes a continuous improvement culture to streamline appropriate processes for maximum efficiency and productivity.Maintains effective relationships with other platform lines, Business Units/Research Units, and enabling lines that facilitates effective portfolio delivery.Completes training assigned by Client and/or EP, as necessary, including general training requirements, SOPs, system, and process related training.Adheres to EP and Client SOPs and processes.

Education and Certification: In general, candidates for this job would have the following levels of experience in Clinical Research/Clinical Operations:Bachelor of Science/equivalent and 2 years’ experience.

Skills and Experience: 

Preferred QualificationsDemonstrated effectiveness working with multiple functions in a professional manner required.Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, database applications).Strong presentation skills, interpersonal skills, as well as a team-oriented approach.Excellent verbal, written, communication and time management skills.Ability to multitask under tight deadlines on several projects with specific and unique requirements, while providing attention to detail and high-quality work.Ability to be flexible, adapt to change, work independently, as well as work as part of a team in a matrix environment.Demonstrated success/results in prior roles including matrix organization.

Language Skills: English Professional Level.

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2022-09-16 00:05:23


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