Research Fellow, Medicine

Overview

The Research Fellow supports the planning and execution of clinical research studies through protocol development, operational management, and engagement with participating study sites.

Roles and Responsibilities

• Develop study protocols and study-related documents.
• Coordinate ethics and regulatory submissions.
• Manage study start-up and day-to-day study operations.
• Monitor study timelines, milestones, and deliverables.
• Engage and support participating study sites throughout study conduct.
• Coordinate communication among investigators, study teams, and stakeholders.
• Ensure compliance with study protocols, GCP, and regulatory requirements.
• Monitor study progress and resolve operational issues.
• Maintain accurate study documentation and project records.
• Prepare study reports, presentations, and other research outputs as required.

Requirements

• Master's degree or PhD in Life Sciences, Biomedical Sciences, Public Health, Clinical Research, or other related health sciences discipline.
• Experience in clinical research, including protocol development, study coordination and site engagement.
• Knowledge of clinical research regulations, ethics, and Good Clinical Practice (GCP) guidelines.
• Strong project management and organisational skills, with the ability to manage multiple studies and timelines.
• Excellent written and verbal communication skills.
• Strong stakeholder management and interpersonal skills to engage investigators and study sites.
• Ability to work independently and collaboratively in a multidisciplinary team.
• Strong analytical and problem-solving skills with attention to detail.
• Experience working in Infectious Disease and/or Antimicrobial resistance is desirable