Senior Clinical Research Associate

Jobgether; Brasil; On-site; BRL 180,000 - 260,000; Full time

Benefits offered by this job

Tailored training courses

Professional mentoring

Exposure to international clinical研究

Career progression opportunities

Job summary

Jobgether is seeking a Senior Clinical Research Associate based in Brazil to oversee site monitoring for Phase II/III trials, train junior CRAs, and ensure protocol adherence across study sites.

You will conduct site qualification visits, initiate sites, perform monitoring, manage data queries, and collaborate with investigators, vendors, and regulatory teams in a globally oriented environment.

Qualifications

• College or university degree in Life Sciences.
• At least 3 years of independent, on-site clinical monitoring experience in Mexico.
• Experience conducting all types of monitoring visits for Phase II and/or Phase III clinical trials.
• Full professional working proficiency in both Spanish and English.
• Willingness and availability to travel as required by study responsibilities.
• Proficiency in Microsoft Office applications.
• Strong planning and organizational skills, with the ability to work effectively in a dynamic team environment.
• Excellent communication, collaboration, and problem-solving abilities.
• Interest and aptitude in training, mentoring, and supporting junior clinical research professionals.
• Experience in oncology or infectious diseases is considered an advantage.

Responsibilities

• Train, mentor, and supervise junior CRAs in their study-level responsibilities.
• Prepare, conduct, and report site selection, initiation, routine monitoring, and closeout visits.
• Deliver training sessions for investigators, site staff, and project teams.
• Work on complex clinical studies, ensuring monitoring activities are completed accurately.
• Perform CRF reviews, source data verification, and data query resolution.
• Manage site communications and relationships with investigators, vendors, and support services.
• Participate in site identification and feasibility research activities.
• Prepare and deliver presentations during Investigator Meetings.
• Support audit preparation and participate in audit findings resolution.
• Assist Regulatory Affairs in obtaining site regulatory documentation.
• Maintain study-specific automated tracking systems.

Skills

Clinical monitoring

Training & mentoring

Regulatory awareness

Communication

Team collaboration

Travel readiness

Planning & organization

Education

Life Sciences degree

Tools

Microsoft Office

Job description

Senior Clinical Research Associate based in Brazil.

Accountabilities

• Train, mentor, and supervise junior CRAs in their study-level responsibilities, supporting their professional development and monitoring performance.
• Prepare, conduct, and report site selection, initiation, routine monitoring, and closeout visits.
• Deliver training sessions for investigators, site staff, and project teams to support consistent study execution and protocol compliance.
• Work on complex clinical studies, ensuring monitoring activities are completed accurately and in accordance with study requirements.
• Perform Case Report Form (CRF) reviews, source document verification, and clinical data query resolution.
• Manage site communications and relationships, serving as a key contact for clinical investigators, vendors, and support services regarding study progress.
• Participate in site identification and feasibility research activities.
• Prepare and deliver presentations during Investigator Meetings.
• Support audit preparation and participation, and contribute to the investigation and resolution of audit findings.
• Assist Regulatory Affairs teams in obtaining and maintaining required site regulatory documentation.
• Maintain study-specific automated tracking systems and ensure relevant information is accurate and up to date.

Requirements

• College or university degree in Life Sciences, or an equivalent combination of education, training, and professional experience.
• At least 3 years of independent, on-site clinical monitoring experience in Mexico, 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 Spanish and English.
• Willingness and availability to travel as required by study responsibilities.
• Proficiency in Microsoft Office applications.
• Strong planning and organizational skills, with the ability to work effectively in a dynamic team environment.
• Excellent communication, collaboration, and problem-solving abilities.
• Interest and aptitude in training, mentoring, and supporting junior clinical research professionals.
• Experience in oncology or infectious diseases is considered an advantage.

Benefits

• Tailored training courses and professional mentoring to support career development.
• Opportunity to develop skills in training, mentoring, and leadership.
• Exposure to complex clinical studies and a variety of clinical research activities.
• Potential career progression toward Lead Monitor responsibilities.
• Opportunity to grow within an international clinical research environment.
• A people-focused culture that emphasizes employee development and professional growth.