Research Assistant

NATIONAL SKIN CENTRE (SINGAPORE) PTE LTD; Singapore; On-site; SGD 20,000 - 60,000; Full time

Job summary

A leading clinical research organization in Singapore is seeking to hire a professional to oversee and coordinate clinical research studies. The role involves managing administrative and operational activities to ensure smooth execution and compliance, leading pre-study preparations, and collaborating with various stakeholders. The ideal candidate should have a Bachelor's degree in sciences or Public Health, and experience in clinical research is advantageous. Good communication skills and resourcefulness are essential for success in this role.

Qualifications

• Experience in clinical research is advantageous.
• Relevant training will be provided when necessary.

Responsibilities

• Lead pre-study preparatory activities to ensure readiness and compliance.
• Coordinate participant recruitment and manage related research activities.
• Collaborate with study sites and research institutes to align workflows.
• Organize and streamline study workflows and assist with consent processes.
• Prepare study applications, reports, and documentation.
• Communicate effectively to document study progress.
• Work independently and collaboratively within cross-functional teams.
• Adapt and apply resourcefulness to resolve challenges.

Skills

Good written and verbal communication skills

Ability to work independently

Resourcefulness

Education

Bachelor’s degree in sciences, Public Health, or equivalent

Job description

Job Summary

You will oversee and coordinate clinical research studies, managing administrative and operational activities to ensure smooth execution and compliance. You will collaborate with multiple stakeholders to drive research outcomes and support informed consent processes.

Responsibilities

• Lead pre-study preparatory activities to ensure readiness and compliance for clinical research studies
• Coordinate participant recruitment and manage related research activities including study monitoring and maintaining accurate participant logs
• Collaborate with other study sites and research institutes to align workflows and share study progress
• Organize and streamline study workflows and assist with the subject informed consent process
• Prepare study applications, reports, and documentation to meet regulatory and institutional requirements
• Communicate effectively in writing and verbally to document study progress and collaborate with team members
• Work independently and collaboratively within cross-functional teams to achieve research objectives
• Adapt and apply resourcefulness to resolve challenges encountered during study execution

Preferred competencies and qualifications

• Bachelor’s degree in sciences, Public Health, or equivalent
• Experience in clinical research is advantageous
• Able to work independently and resourceful
• Good witten and verbal communication skills
• Relevant training will be provided when necessary