Clinical Research Specialist

Location: Singapore
Department: Clinical Research

• About the Role

We are seeking a Clinical Research Specialist to support the planning, coordination, and execution of clinical trials within our Clinical Research Organisation (CRO) in Singapore. You will ensure studies are conducted in compliance with regulatory requirements, Good Clinical Practice (GCP), and company standards.

• Key Responsibilities

• Assist in the design, initiation, monitoring, and close-out of clinical trials.
• Ensure adherence to GCP, ICH guidelines, and local regulatory requirements (HSA).
• Collect, verify, and manage clinical trial data for accuracy and integrity.
• Support communication with investigators, study sites, and regulatory bodies.
• Contribute to preparation of study documentation, reports, and submissions.

• Qualifications
• Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or related field.
• 2–4 years’ experience in clinical research or within a CRO environment.
• Strong knowledge of GCP, ICH, and Singapore HSA regulations.
• Excellent organizational, analytical, and communication skills.
• Ability to work independently and as part of a cross-functional team.

Disclaimer: This is a sample job listing created for demonstration purposes only. It is not an actual job advertisement.

Disclaimer: This is a sample company profile created for demonstration purposes only. The information provided does not represent a real company, and any resemblance to actual organizations, past or present, is purely coincidental.