Research Assistant - 1 year contract, Renewable

National Healthcare Group Polyclinics; Singapore; On-site; SGD 35,000 - 55,000; Full time

Job summary

A healthcare institution in Singapore is seeking a Research Assistant for a 1-year renewable contract. The role involves assisting with grant funding management, coordinating studies, and ensuring data integrity. The ideal candidate holds a Bachelor's degree in a life science discipline and has experience in a healthcare setting. Strong organizational and English communication skills are essential.

Qualifications

• 1-2 years of working experience in healthcare setting preferred.
• Prior experience in clinical research is advantageous.
• Knowledgeable in Good Clinical Practice and regulatory affairs preferred.

Responsibilities

• Assist PI in managing grant funding and regulatory approvals.
• Oversee coordination of studies with multiple sites.
• Monitor and report all adverse events to the Principal Investigator.

Skills

Proficient in Microsoft Office applications

Advanced English language and writing skills

Meticulous with good organization skills

Ability to work both as part of a team and independently

Education

Bachelor Degree in a life science related discipline

Job description

Overview

Research Assistant - 1 year contract, Renewable

Institution: National Healthcare Group Polyclinics

Family Group: Administration

Responsibilities

• Assist PI in managing applicable grant funding, regulatory and IRB approvals, for the assigned projects, including corresponding with the granting body/regulatory authority/IRB.
• Manage approved study budget, where applicable, including tracking the utilization of budget.
• Oversee coordination of studies with multiple sites, where applicable.
• Assist to monitor progress of study and coordinate regular reviews with the study team and CRU.
• Assist PI in preparation of study-related presentations/materials.
• Participate in the evaluation of research results where required.
• Perform screening activities according to protocol eligibility criteria and assist in recruitment.
• Schedule study visits and ensure visit schedules are adhered to. Follow up and monitor participants in accordance with study protocol.
• Be cognizant of current regulatory, ethical and institutional requirements, and perform delegated protocol-specific activities according to the guidelines.
• Monitor and report all adverse/unanticipated events and abnormalities/protocol deviations to the Principal Investigator and CRU. Ensure these events are reported accordingly to granting body, regulatory authority and IRB as applicable.
• Maintain research data integrity and appropriate study documentation.
• Work closely with research team for smooth coordination of research projects.
• Meet with the Principal Investigator/research team members to discuss the conduct of the study and review study data.

Job Requirements

• Bachelor Degree in a life science related discipline
• Preferably with 1-2 years of working experience in healthcare setting
• Prior experience in clinical research would be advantageous.
• Proficient in Microsoft Office applications
• Advanced English language and writing skills
• Knowledgeable in Good Clinical Practice, clinical trials and regulatory affairs and medical and research ethics preferred
• Knowledge in medical and research terminology preferred
• Meticulous with good organization, coordination and administrative skills
• Ability to integrate, interpret and summarize and present data from a variety of sources in a clear, accurate and concise manner
• Ability to work both as part of a team and independently

We regret to inform that only shortlisted applicants will be notified.