Clinical Research Associate I or II

ICON; São Paulo; Presencial; BRL 90 000 - 130 000; Tempo integral

Resumo da oferta

ICON Plc seeks a Clinical Research Associate to join our sponsor-dedicated team in São Paulo, overseeing and coordinating clinical trials, ensuring regulatory compliance, and collecting critical data.

You will build relationships with investigators and sites, monitor study progress, manage queries, and support feasibility studies while traveling up to 60% and maintaining study documentation.

ICON offers competitive salary and benefits and a commitment to inclusion and workplace accessibility.

Qualificações

• Knowledge of ICH-GCP guidelines and the ability to review and evaluate medical data.
• Excellent written and verbal communication in English.
• Strong interpersonal skills to manage queries and collaborate with sites.

Responsabilidades

• Coordinate all activities for setting up and monitoring a study, with accurate study status reports and documentation.
• Run sponsor-generated queries efficiently and contribute to study cost efficiency; assist in feasibility studies and documentation review for new proposals.
• Develop and maintain collaborative relationships with investigators, site staff, and stakeholders; ensure patient safety and regulatory compliance.

Conhecimentos

ICH-GCP knowledge

English proficiency

Travel readiness

Communication skills

Formação académica

University degree in medicine/science

Descrição da oferta de emprego

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

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.

As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.

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 license

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