Clinical Research Associate II - São Paulo/Campinas/Rio de Janeiro

Pharmaceutical Research Associates, Inc; Brasil; Presencial; BRL 80.000 - 120.000; Tempo integral

Resumo da oferta

A leading clinical research organization in Brazil is seeking a Clinical Research Associate II to oversee clinical trials and ensure data integrity. The ideal candidate will possess a Bachelor's degree in life sciences and relevant experience, with strong leadership and communication skills. This role offers competitive salary and benefits, including various health insurance options and annual leave entitlements.

Serviços

Various annual leave entitlements

Health insurance offerings

Competitive retirement planning

Global Employee Assistance Programme

Flexible country-specific optional benefits

Qualificações

• Experience as Clinical Research Associate with on-site monitoring activities.
• In-depth knowledge of ICH-GCP guidelines and regulatory requirements.
• Advanced level of English.

Responsabilidades

• Conduct site qualification, initiation, monitoring, and close-out visits for trials.
• Ensure protocol compliance, data integrity, and patient safety.
• Collaborate with investigators and site staff for smooth study conduct.
• Perform data review and resolution of queries.

Conhecimentos

Leadership

Communication

Problem-solving

Organizational skills

Formação académica

Bachelor's degree in life sciences, nursing, pharmacy, or related field

Advanced degree preferred

Descrição da oferta de emprego

Overview

We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

Responsibilities

What you will be doing:

• Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
• Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
• Collaborating with investigators and site staff to facilitate smooth study conduct.
• Performing data review and resolution of queries to maintain high-quality clinical data.
• Contributing to the preparation and review of study documentation, including protocols and clinical study reports.

Qualifications

• Bachelor's degree in life sciences, nursing, pharmacy, or a related field. Advanced degree preferred.
• Experience as Clinical Research Associate and with on-site monitoring activities.
• In-depth knowledge of ICH-GCP guidelines, regulatory requirements, and clinical trial processes.
• Strong leadership and mentoring skills, with the ability to manage and motivate CRAs and site staff effectively.
• Excellent communication, organizational, and problem-solving skills, with a proactive approach to managing site performance and resolving issues.
• Advanced level of English.

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 maximise savings and plan with confidence for the years ahead
• Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised 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, subsidised travel passes, health assessments, among others

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

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, colour, 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 through the form below. https://careers.iconplc.com/reasonable-accommodations

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.