Clinexa is a Clinical Research Organization (CRO) dedicated to supporting pharmaceutical, biotechnology, and healthcare partners in the successful delivery of clinical trials and research programs. The company fosters a collaborative and fast-paced environment where professionals are empowered to contribute to innovative research, uphold high standards of quality and compliance, and grow their careers within the evolving clinical research and life sciences industry.

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.

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