Clinical Research Associate II

Jobgether; Brasil; On-site; BRL 90,000 - 150,000; Full time

Job summary

Jobgether, on behalf of a partner company, seeks a Clinical Research Associate II based in Brazil. The role covers on-site monitoring, study startup support, and regulatory submissions coordination across therapeutic indications.

You will collaborate with investigators, internal teams, vendors, and regulatory specialists to ensure quality standards, data integrity, and timely study progress. Travel is required; oncology experience is a plus.

Qualifications

• Bachelor degree in Life Sciences or equivalent.
• On-site monitoring experience in Argentina.
• Experience in Phase II/III monitoring visits.
• Fluent in English and Spanish.
• Proficient with Microsoft Office.
• Strong planning and organization in a dynamic team.
• Excellent communication and collaboration with sites and teams.
• Willingness to travel as required.
• Experience in oncology preferred.

Responsibilities

• Conduct and document on-site monitoring visits meeting quality standards.
• Support study startup and site feasibility.
• Perform CRF reviews and data query resolution.
• Manage site communications with investigators and staff.
• Coordinate with internal teams and external vendors.
• Communicate study progress and issues to project teams.
• Prepare and gather documentation for regulatory submissions.
• Ensure timely execution of activities across studies.

Skills

On-site monitoring

English proficiency

Spanish proficiency

Planning & organization

Communication skills

Analytical thinking

Travel willingness

Oncology experience

Education

Life Sciences degree

Tools

MS Office

Job description

This position is listed on behalf of a partner company, which manages all applications and next steps. Our partner is looking for a Clinical Research Associate II based in Brazil.

As a Clinical Research Associate II, you will contribute to the successful delivery of clinical trials across a range of therapeutic indications. You will conduct on-site monitoring activities, support study startup, and help ensure that clinical research is performed in accordance with established quality standards. Working closely with clinical sites, investigators, internal project teams, vendors, and regulatory specialists, you will help maintain effective communication and study progress. Your responsibilities will span monitoring visits, source document verification, clinical data review, and query resolution. You will also support feasibility activities and the preparation of regulatory submission documentation. This opportunity offers exposure to different therapeutic areas, allowing you to strengthen your clinical research expertise and continue developing your career in a quality-focused international environment.

Accountabilities:

• Conduct and document all types of on-site clinical monitoring visits, ensuring study activities meet applicable quality standards and requirements.

• Participate in study startup activities and feasibility research to support effective site selection and study preparation.

• Perform Case Report Form (CRF) reviews, source document verification, and clinical data query resolution.

• Manage site communications and relationships, maintaining effective coordination with investigators and site personnel.

• Serve as a point of contact for internal support services and external vendors, helping address study-related needs.

• Communicate regularly with internal project teams regarding site activities, study progress, and relevant issues.

• Collaborate with regulatory teams to prepare and gather documentation required for clinical study submissions.

• Support the consistent and timely execution of clinical research activities across assigned studies and therapeutic indications.

Requirements:

• College or university degree in Life Sciences, or an equivalent combination of education, training, and professional experience.

• Independent on-site clinical monitoring experience in Argentina, as specified in the original posting.

• Experience conducting all types of monitoring visits for Phase II and/or Phase III clinical trials.

• Full professional working proficiency in both English and Spanish.

• Proficiency in Microsoft Office applications.

• Strong planning and organizational skills, with the ability to manage responsibilities in a dynamic team environment.

• Effective communication and collaboration skills, with the ability to work with clinical sites, internal teams, and external partners.

• Strong analytical thinking and problem-solving abilities.

• Willingness and availability to travel as required by clinical study activities.

• Experience in oncology is preferred.

Benefits:

• Opportunity to develop clinical research skills through involvement in a variety of monitoring activities.

• Exposure to clinical studies across different therapeutic indications.

• Opportunity to broaden therapeutic area knowledge and build expertise in clinical research.

• Professional development within an established clinical research environment that emphasizes quality and timely delivery.

Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time.

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