About this role
The Clinical Research Associate will oversee and coordinate clinical trials, ensuring compliance with regulations and collecting critical data. Responsibilities include coordinating study activities, maintaining documentation, and developing relationships with stakeholders.
Candidates should have at least 2 years of monitoring experience as a CRA and a university degree in medicine, science, or a related field. Knowledge of ICH-GCP guidelines and excellent communication skills in English are also required.
What they're looking for
Clinical TrialsData AnalysisMonitoring ExperienceICH-GCP GuidelinesCommunication SkillsStakeholder ManagementRegulatory ComplianceMedical Data Evaluation
Frequently asked questions
What does a Clinical Research Associate at ICON plc do?
The Clinical Research Associate will oversee and coordinate clinical trials, ensuring compliance with regulations and collecting critical data. Responsibilities include coordinating study activities, maintaining documentation, and developing relationships with stakeholders. Candidates should have at…
What skills does this Clinical Research Associate role need?
Key skills for this role include Clinical Trials, Data Analysis, Monitoring Experience, ICH-GCP Guidelines, Communication Skills, Stakeholder Management.
How much does a Clinical Research Associate at ICON plc pay?
The employer did not list a salary for this role. Most similar Singapore roles publish their band on the job page.
Is this Clinical Research Associate role remote, hybrid, or on-site?
This role is on-site, based in Singapore.
How do I apply for this Clinical Research Associate role?
You can apply directly on ICON plc's careers page. ApplyLah can tailor your résumé and cover letter to this exact role in seconds first.