Clinical Research Coordinator

PICKPROS PTE. LTD.; Singapore; Vor Ort; SGD 50.000 - 70.000; Vollzeit

Zusammenfassung

PICKPROS PTE. LTD. is seeking a Clinical Research Coordinator to oversee end-to-end trial activities within a Singapore-based team.

The role involves coordinating start-up processes, daily trial operations, and close-out activities while ensuring adherence to protocols and regulatory standards. You will assist with patient screening, consent and assessments, and help maintain trial data and documentation. The successful candidate will support adverse event reporting, invoicing and trial-related

Qualifikationen

• Experience coordinating clinical trials or related research activities.
• Familiarity with GCP guidelines and regulatory requirements.
• Strong data management and documentation skills.
• Ability to support site monitoring visits and audits.

Aufgaben

• Coordinate clinical trials, including study start-up, daily activities and close-out.
• Ensure compliance with study protocols, GCP guidelines and regulatory requirements.
• Support patient screening, informed consent, study assessments and timely adverse event reporting.
• Maintain accurate study data, trial documents and specimen records, and support monitoring visits and audits.
• Track trial expenses and support timely invoicing and research account closure

Kenntnisse

Clinical trials coordination

GCP compliance

Regulatory knowledge

Data management

Patient screening

Jobbeschreibung

Clinical Research Coordinator

1. Coordinate clinical trials, including study start-up, daily activities and close-out.

2. Ensure compliance with study protocols, GCP guidelines and regulatory requirements.

3. Support patient screening, informed consent, study assessments and timely adverse event reporting.

4. Maintain accurate study data, trial documents and specimen records, and support monitoring visits and audits.

5. Track trial expenses and support timely invoicing and research account closure