Senior Clinical Research Associate - Oncology - Brazil - Remote

Worldwide Clinical Trials; Brasília; On-site; BRL 120,000 - 180,000; Full time

Job summary

Worldwide Clinical Trials seeks a seasoned Clinical Research Associate to monitor sites, qualify and initiate visits, oversee interim monitoring, and guide study close‑out across multiple trials.

Bring 5+ years of CRA experience, travel willingness, and a 4‑year degree or RN/BSN. Proficiency with MS Office, CTMS and EDC is required to ensure compliance and high data quality across studies.

Qualifications

• 5+ years of experience as a Clinical Research Associate.
• 4-year university degree or RN/BSN in Nursing.
• Willingness to travel required.

Responsibilities

• Responsible for site qualification, initiation, interim monitoring, site management, and study close‑out visits.
• Provide mentoring and guidance to less experienced CRAs and site staff when needed.
• Document site visit findings via written reports.
• Assess, monitor, and train study site staff on protocol adherence as required.
• Review study subject safety information and informed consent.
• Conduct source document verification for compliance, patient safety, and veracity of data.
• Review CRFs using paper or electronic data capture systems and assist sites with data query resolution.
• Provide applicable updates for site-related documentation for filing in the Trial Master File (TMF).
• Ensure site compliance with IP receipt, accountability and return or destruction.
• Conduct accompanied site visits for assessment or training of other CRAs as requested and appropriate.

Skills

Site monitoring

Protocol adherence

Data verification

Mentoring

Documentation

MS Office

CTMS

EDC Systems

Education

Bachelor's degree in life sciences or RN/BSN

Tools

MS Office

CTMS

EDC Systems

Job description

Who We Are

We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.

Why Worldwide

We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands‑on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day.

What The Clinical Operations Department Does At Worldwide

Clinical Research Associates (CRAs) play a vital role in ensuring our clinical research programs are executed with the quality and excellence our sponsors expect and the care and passion patients deserve. They are the backbone of every strong CRO, helping drive breakthrough scientific research and playing a lead role on every clinical trial.

What You Will Do

• Responsible for site qualification, initiation, interim monitoring, site management, and study close‑out visits.
• Provide mentoring and guidance to less experienced CRAs and site staff when needed.
• Document site visit findings via written reports.
• Assess, monitor, and train study site staff on protocol adherence as required.
• Review study subject safety information and informed consent.
• Conduct source document verification for compliance, patient safety, and veracity of data.
• Review CRFs using paper or electronic data capture systems and assist sites with data query resolution.
• Provide applicable updates for site-related documentation for filing in the Trial Master File (TMF).
• Ensure site compliance with IP receipt, accountability and return or destruction.
• Conduct accompanied site visits for assessment or training of other CRAs as requested and appropriate.

What You Will Bring To The Role

• Excellent interpersonal, oral, and written communication skills in English.
• Superior organizational skills with attention to details.
• 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 RN/BSN in Nursing.
• Willingness to travel 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 know that when our employees feel appreciated and included, they can be more creative, innovative, and successful. We’re on a mission to hire the very best and are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. 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.