Study Support Assistant - Recife

Pharmaceutical Research Associates, Inc; Brasil; Presencial; BRL 20.000 - 80.000; Tempo integral

Resumo da oferta

A leading clinical research organization is seeking a Study Support Assistant in Brazil to provide administrative support for clinical trials. In this diverse role, you will help coordinate meetings, manage documentation, and ensure compliance with regulatory requirements. Ideal candidates have strong organizational skills, excellent communication abilities, and a bachelor's degree in health or life sciences.

Serviços

Health insurance options

Retirement planning options

Global Employee Assistance Programme

Flexible benefits like childcare vouchers and gym discounts

Annual leave entitlements

Qualificações

• Bachelor's degree in health, life sciences, or related fields required.
• Experience in clinical research or administrative roles is preferred.
• Fluent in the local language and proficient in English.

Responsabilidades

• Provide administrative and operational support for clinical trials.
• Manage study-related correspondence and documentation.
• Assist with the preparation and distribution of study documents.

Conhecimentos

Organizational skills

Attention to detail

Communication

Interpersonal skills

Proficiency in Microsoft Office

Formação académica

Bachelor's degree in health, life sciences, or related fields

Descrição da oferta de emprego

Overview

As a Study Support Assistant, you will join the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

Responsibilities

We are seeking a Study Support Assistant to join our diverse and dynamic team. In this role at ICON, you will provide administrative and operational support for clinical trials, contributing to the development of innovative treatments and therapies.

What you will be doing

• Assisting with the preparation and distribution of study documents, including protocols, informed consent forms, and regulatory submissions.
• Coordinating study-related meetings and maintaining meeting minutes and action items.
• Managing study-related correspondence, including emails and phone calls.
• Supporting study teams in maintaining study files and documentation, ensuring regulatory compliance and adherence to company procedures.
• Assisting with the tracking and management of study-related materials and supplies.

Qualifications

• Bachelor's degree in health, life sciences, or related fields.
• Previous administrative or clerical experience in clinical research.
• Strong organizational skills and attention to detail.
• Excellent communication and interpersonal skills, capable of working effectively in a team.
• Proficiency in Microsoft Office (Word, Excel, Outlook).
• Fluent in the local language and proficient in English.
• Based in Recife/PE region.

What ICON can offer you

Our success depends on our people. We prioritize building a diverse culture that rewards high performance and nurtures talent. Along with a competitive salary, ICON offers various benefits focused on well-being and work-life balance, including:

• Annual leave entitlements
• Health insurance options
• Retirement planning options
• Global Employee Assistance Programme (TELUS Health)
• Life assurance
• Flexible benefits such as childcare vouchers, bike schemes, gym discounts, travel passes, and health assessments

Visit our careers website to learn more about working at ICON: https://careers.iconplc.com/benefits

At ICON, inclusion & belonging are core to our culture. We are committed to providing an accessible environment for all candidates and a workplace free of discrimination. If you require reasonable accommodations during the application process or for the role, please let us know through the provided form: https://careers.iconplc.com/reasonable-accommodations

If you're interested but unsure if you meet all requirements, we encourage you to apply. You may be exactly what we're looking for at ICON.