Senior Clinical Research Associate-Oncology-Brazil (Remote)

Worldwide Clinical Trials; Brasília; Presencial; BRL 120 000 - 180 000; Tempo integral

Resumo da oferta

Worldwide Clinical Trials in Brazil is seeking a seasoned Clinical Research Associate to oversee research activities at sites participating in our clinical studies.

You will identify potential sites, support start-up activities, train site staff, and ensure proper data capture and safety reporting, with travel regionally as needed.

The role focuses on regulatory compliance, site management, and close collaboration with sponsors to ensure studies are conducted on time and to high quality standards.

Qualificações

• Excellent English communication skills (oral and written).
• Strong organizational abilities with attention to detail.
• Ability to work with little or no supervision.
• Proficiency in Microsoft Office, CTMS, and EDC Systems.

Responsabilidades

• Manage research activities at participating sites.
• Oversee start-up activities, collect regulatory documents, and support contracts/budgets.
• Train sites to collect data and report safety events.
• Conduct study initiation visits (SIVs).
• Ensure regulatory compliance and informed consent across sites.

Conhecimentos

English communication

Organizational skills

Independent work

Formação académica

Bachelor's degree

Nursing degree

Ferramentas

CTMS

EDC Systems

MS Office

Descrição da oferta de emprego

What You Will Do

• Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects.
• Typically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets, training the sites to collect data properly and report any potential safety-related events, managing the site's activities during study maintenance, and closing down research activities at the sites once the study has concluded.
• Conduct study initiation visits (SIVs).
• While most of the site management efforts will be performed remotely, you will be required to ensure compliance with obtaining informed consent, reporting potential safety-related events, and adhering to all applicable regulatory requirements.

What You Will Bring To The Role

• Excellent interpersonal, oral, and written communication skills in English.
• Superior organizational skills with attention to detail.
• Ability to work with little or no supervision.
• Proficiency in Microsoft Office, CTMS, and EDC Systems.

Your Experience

• 5+ years of experience as a Clinical Research Associate.
• 4-year university degree OR Nursing Degree.
• Experience in Oncology and Rare Disease is required.
• Fluent in written and verbal English required.
• Candidates must reside in Brazil.
• Willingness to travel regionally required.

Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law.