Study Coordinator // Rio de Janeiro, Brazil

R&D Partners; Rio de Janeiro; Vor Ort; BRL 33.000 - 47.000; Teilzeit

Benefits dieser Stelle

Onsite in Rio de Janeiro

Part-time hours

Zusammenfassung

R&D Partners is seeking a Clinical Research Coordinator to support clinical trial activities onsite in Rio de Janeiro, Brazil. This role supports investigators and study teams in a fast-paced environment and requires fluency in Portuguese.

The position is part-time (16 hours per week) with a 6-month project duration and ASAP start. Candidates must have right to work in Brazil and experience in clinical research coordination.

Qualifikationen

• Native Portuguese
• Experience in clinical research coordination
• Available for 16 hours/week
• Project duration: 6 months
• ASAP start date

Aufgaben

• 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.

Kenntnisse

Portuguese fluency

Clinical research coordination

Organizational and communication

Jobbeschreibung

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

For more information, please contact Terrah-Leigh Pietersen.