Parexel

Feasibility Specialist - FSP

Parexel

MexicoFull TimeOther
📍 MexicoPosted January 21, 1970

Job Description

When our values align, there's no limit to what we can achieve.

At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

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

Originally posted on Himalayas