Research Assistant

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

Job summary

A clinical research facility in Singapore is seeking a candidate to oversee and coordinate clinical research studies. The role involves managing administrative and operational activities, collaborating with multiple stakeholders to ensure smooth execution and compliance. The ideal candidate should possess a Bachelor’s degree in sciences or Public Health and have experience in clinical research. Key responsibilities include leading preparatory activities, participant recruitment, and maintaining study documentation. Effective communication skills are essential.

Qualifications

• Bachelor’s degree in sciences, Public Health, or equivalent.
• Experience in clinical research is advantageous.
• Able to work independently and resourceful.
• Good written and verbal communication skills.

Responsibilities

• Lead pre-study preparatory activities for clinical research studies.
• Coordinate participant recruitment and manage research activities.
• Collaborate with other study sites to align workflows.
• Organize study workflows and assist with informed consent.
• Prepare study applications and reports for regulatory compliance.
• Document study progress and collaborate with team members.
• Work independently and collaboratively to achieve objectives.
• Adapt to resolve challenges during study execution.

Skills

Independent work

Resourcefulness

Communication skills

Education

Bachelor’s degree in sciences or Public Health

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