Research Fellow (Medicine)

National University of Singapore; Singapore; Presencial; SGD 70.000 - 110.000; Jornada completa

Descripción de la vacante

The National University of Singapore, Yong Loo Lin School of Medicine, seeks a Research Fellow to support clinical studies through protocol development, regulatory submissions, and hands-on study coordination at Kent Ridge Campus.

You will develop study documents, manage ethics submissions, monitor timelines, engage study sites, ensure GCP compliance, and prepare reports and outputs for investigators and stakeholders.

Formación

• PhD in Life Sciences, Biomedical Sciences, Public Health, Clinical Research, or related health sciences.
• Experience in clinical research, including protocol development and study coordination.
• Knowledge of clinical research regulations, ethics, and GCP guidelines.
• Strong project management and organisational skills for multiple studies and timelines.
• Excellent written and verbal communication.
• 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.

Responsabilidades

• 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.

Conocimientos

Clinical research

GCP knowledge

Project management

Communication

Stakeholder management

Team collaboration

Analytical thinking

Educación

PhD in Life Sciences / Biomedical Sciences / Public Health / Clinical Research

Descripción del empleo

University-Level Unit: Yong Loo Lin School of Medicine

Faculty/Department-Level Unit: Medicine

Employee Category: Research Staff

Location_ONB: Kent Ridge Campus

Posting Start Date: 24/07/2026

Job Description

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

Primary responsibilities and duties

• 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.

Jobscope and Responsibilities

• Study protocols and study documents completed within agreed timelines.
• Ethics and regulatory submissions submitted on time.
• Study start-up milestones achieved according to project timelines.
• Study operations managed efficiently with minimal delays.
• Regular engagement and timely communication with participating study sites.
• Recruitment and study milestones tracked and monitored effectively.
• Operational issues identified and resolved within agreed timelines.
• Compliance with GCP, institutional, and regulatory requirements.
• Accurate, complete, and audit-ready study documentation maintained.
• Timely submission of study progress reports and project updates.
• Positive feedback from Principal Investigators and participating study sites.

Qualifications

• PhD in Life Sciences, Biomedical Sciences, Public Health, Clinical Research, or other related health sciences discipline.
• Experience in clinical research, including protocol development and study coordination.
• 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.