Key Facts

Remote From:

Brazil , Argentina , Mexico

Full time

English

Hard Skills

Other Skills

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Microsoft Excel
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Microsoft PowerPoint
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Quick Learning
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Microsoft Word
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Non-Verbal Communication
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Multitasking
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Time Management
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Teamwork
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Detail Oriented
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Social Skills
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Problem Solving

Parexel

Pharmaceuticals

About Parexel

Parexel is among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help life-saving treatments reach patients faster. Leveraging the breadth of our clinical, regulatory and therapeutic expertise, our team of more than 21,000 global professionals collaborates with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere. Our depth of industry knowledge and strong track record gained over the past 40 years is moving the industry forward and advancing clinical research in healthcare’s most complex areas, while our innovation ecosystem offers the best solutions to make every phase of the clinical trial process more efficient. With the people, insight and focus on operational excellence, we work With HeartTM every day to treat patients with dignity and continuously learn from their experiences, so every trial makes a difference. For more information, visit parexel.com. Community Guidelines Because Parexel’s social media channels are open to the general public and employees, we are not responsible for views expressed other than our own. However, we do not tolerate posts that are: • Abusive, harassing or threatening to others. • Defamatory, offensive, obscene, vulgar or depicting violence. • Hateful targeting by race/ethnicity, age, color, creed, religion, gender, sexual preference or orientation, nationality or political beliefs. • Sexually explicit or pornographic. • Fraudulent, deceptive, libelous, misleading or unlawful. • Referencing criminal or illegal activity. • Spamming. We reserve the right to remove any comments that do not adhere to our guidelines as well as report users who violate the rules of our page.

Company type: XLarge

Industry: Pharmaceuticals

Founded: 2018

Company size: 10001

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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