Clinical Research Associate I or II

ICON Strategic Solutions; Brasil; Presencial; BRL 120 000 - 180 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Annual leave entitlements

Health insurance offerings

Retirement planning options

Global Employee Assistance Programme

Life assurance

Resumo da oferta

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re seeking a Clinical Research Associate to join our team in São Paulo. You will oversee and coordinate clinical trials, ensuring regulatory compliance and high-quality data collection.

Responsibilities include coordinating study setup and monitoring, reviewing documentation, and maintaining study status reports. The role requires a medicine/science degree, strong ICH-GCP knowledge, and travel up to 60%

Qualificações

• Knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data.
• Excellent written and verbal communication in English.
• Willingness and ability to travel at least 60% of the time (international and domestic) with a valid driver’s license.

Responsabilidades

• Coordinate all activities for setting up and monitoring a study, including reporting and documentation.
• Run sponsor-generated queries efficiently and support study cost efficiency and feasibility studies for new proposals.
• Develop and maintain strong, collaborative relationships with stakeholders, investigators, and site staff.
• Ensure patient safety by adhering to ICON’s procedures, protocols, and regulatory requirements.

Conhecimentos

ICH-GCP knowledge

English communication

travel willingness

Formação académica

University degree in medicine/science

Descrição da oferta de emprego

Clinical Research Associate I or II - São Paulo (FSP - Sponsor Dedicated)

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

We are currently seeking a Clinical Research Associate to join our diverse and dynamic team at ICON Plc. As a key member of our research department, you will be responsible for overseeing and coordinating clinical trials, ensuring compliance with regulations, and collecting and analyzing critical data.

What You Will Be Doing

• Working independently and actively to coordinate all activities for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation
• Running sponsor generated queries efficiently and taking responsibility for study cost efficiency; you will also participate in the preparation and review of study documentation and feasibility studies for new proposals as required.
• Develop and maintain strong, collaborative relationships with key stakeholders, clinical investigators, and site staff.
• Ensure patient safety by ensuring compliance with ICON’s procedures, protocols, and regulatory requirements.

Your profile

• University degree in medicine, science, or equivalent
• Knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data
• Excellent written and verbal communication in English
• Good social skills enabling you to deal with queries in a timely manner
• Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid drivers licence

What ICON Can Offer You

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our Benefits Examples Include

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs.
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here