Study Coordinator / Rio de Janeiro, Brazil

R Dpartners; Rio de Janeiro; On-site; BRL 40,000 - 60,000; Part time

Job summary

R&D Partners is seeking a Clinical Research Coordinator to support clinical trial activities onsite in Rio de Janeiro, Brazil. This part-time role requires fluency in Portuguese and immediate availability, with a 16-hour work week.

The position supports patients, investigators, and study teams in a fast-paced trial environment. A right to work in Brazil is required, and the project duration is 6 months with ASAP start.

Qualifications

• Native proficiency in Portuguese.
• Experience in clinical research coordination.
• Strong organizational and communication skills.
• Availability to work 16 hours per week.

Responsibilities

• Perform trial procedures as delegated by the Principal Investigator.
• Prescreen patients and obtain informed consent from eligible subjects.
• Enter data into Electronic Data Capture (EDC) systems.
• Schedule subject visits within the designated visit window.

Skills

Portuguese proficiency

Clinical research coordination

Organization & communication

16 hours/week availability

Tools

Electronic Data Capture (EDC) systems

Job description

Help advance clinical research by supporting patients, investigators, and study teams in a fast-paced trial environment.

R&D Partners is seeking a Clinical Research Coordinator to support clinical trial activities onsite in Rio de Janeiro, Brazil. This role is ideal for candidates with experience in clinical research and fluency in Portuguese. The position requires immediate availability and offers part-time hours.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

• Perform trial procedures as delegated by the Principal Investigator.
• Prescreen patients and obtain informed consent from eligible subjects.
• Enter data into Electronic Data Capture (EDC) systems.
• Schedule subject visits within the designated visit window.

Key Skills and Requirements:

• Native proficiency in Portuguese.
• Experience in clinical research coordination.
• Strong organizational and communication skills.
• Availability to work 16 hours per week.

Additional Details:

• Project Duration: 6 months
• Anticipated Start Date: ASAP