Feasibility Specialist - FSP
Primary Location: Mexico, Remote Additional Locations: Argentina, Remote; Brazil, Remote Job ID R0000041013 Category Clinical Trials
About this Role
Parexel FSP is hiring 2 Feasibility Specialists - 1 in Argentina and 1 in Mexico, Brazil or Argentina
Role Responsibilities:
Acts as a supportive team member for Regional Intelligence
Performs tasks for multiple Site Intelligence and Feasibility projects.
Able to manage a high volume of complex studies and sites
Works under close supervision of Regional Intelligence Team Lead, and where needed the Feasibility Specialist Point of Contact (POC)
Contributes to executing Site Feasibility plans and presenting the data to colleagues.
Supports the Feasibility Strategy & Analytics Lead (FSAL) to ensure knowledge of goals, scope and requirements of the Site Feasibility project are understood, and ensures that high quality results are executed and delivered.
Applies skills and discipline knowledge to OARS and Regional Intelligence development projects
Promotes a continuous improvement culture to streamline appropriate processes for maximum efficiency and productivity
Develops and maintains internal processes aimed to optimize country & site selection activities
Creates awareness by working as a cross functional team leader to deliver data, analytics and regional site intelligence initiatives across a broad spectrum of stakeholders, both internal and external
Contribution to wider initiatives, both technology and process improvement components
Runs operational and technical aspects of large global projects and assists with other Company systems activities related to site intelligence
Maintains effective relationships with other platform lines, Business Units/Research Units, and enabling lines that facilitates effective portfolio delivery
Partners with GSSO and CD&O teams to improve overall study start up metrics and implement simple processes
QUALIFICATIONS
BASIC QUALIFICATIONS
In general, candidates for this job would have the following levels of experience in Clinical Research/Clinical Operations: 2-3 years
Manager/Senior Associate: Experience working in the pharmaceutical industry or CRO in a similar role
Effective verbal and written communication skills in relating to colleagues and stakeholders both inside and outside of the organization
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
PREFERRED QUALIFICATIONS
Experience in a clinical research organization and related therapeutic specialties with familiarity in principles, concepts, practices and standards.
Prior feasibility experience
An eye for detail and ability to problem solve operational challenges and provide high level insights to a multidisciplinary team.
Proficiency in Microsoft SharePoint
Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, database applications)
A quick learner with the desire to contribute and support the design and implementation of analytical insights and management of data platforms.
Demonstrated success/results in prior roles including matrix organization
Organizational Relationships:
Collaborates across functional lines within CD&O, R&D, Contract Research Organizations (CROs), Legal and Quality Representatives, and Functional Service Providers (FSPs).
Works under supervision of Regional Intelligence Team Lead
Global Study Manager, Start-Up Project Manager, Global Study Clinician
Local Site Relationship Partners and Director Clinical Site Operations (DCSO), Clinical Trials Manager and other Local Roles
Global Quality and Event representatives
Feasibility Strategy & Analytics Lead (FSAL) & Due Diligence Lead
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