CRA II

ICON; Singapore; On-site; SGD 20,000 - 60,000; Full time

Job summary

A leading clinical research organization in Singapore is looking for a Clinical Research Associate to conduct site visits, ensure compliance, and support study documentation. Candidates must hold a Bachelor's degree, possess at least 2 years of relevant experience, and have strong organizational skills. The role requires the ability to travel extensively and offers competitive benefits including health insurance and retirement planning options.

Benefits

Various annual leave entitlements

Health insurance offerings

Competitive retirement planning

Global Employee Assistance Programme

Life assurance

Flexible optional benefits

Qualifications

• Minimum of 2 years of experience as a Clinical Research Associate.
• In-depth knowledge of clinical trial processes and regulations.
• Ability to travel at least 60% of the time and possess a valid driver’s license.

Responsibilities

• Conduct site qualification, initiation, monitoring, and close‑out visits for clinical trials.
• Ensure protocol compliance, data integrity, and patient safety throughout the trial process.
• Collaborate with investigators and site staff to facilitate smooth study conduct.
• Perform data review and resolve queries to maintain high quality data.
• Contribute to the preparation and review of study documentation.

Skills

Organizational skills

Communication skills

Attention to detail

Education

Bachelor's degree in a scientific or healthcare-related field

Job description

What you will be doing

• Conduct site qualification, initiation, monitoring, and close‑out visits for clinical trials.
• Ensure protocol compliance, data integrity, and patient safety throughout the trial process.
• Collaborate with investigators and site staff to facilitate smooth study conduct.
• Perform data review and resolve queries to maintain high‑quality clinical data.
• Contribute to the preparation and review of study documentation, including protocols and clinical study reports.

Your profile

• Bachelor's degree in a scientific or healthcare‑related field.
• Minimum of 2 years of experience as a Clinical Research Associate.
• In‑depth knowledge of clinical trial processes, regulations, and ICH‑GCP guidelines.
• Strong organizational and communication skills, with attention to detail.
• Ability to work independently and collaboratively in a fast‑paced environment.
• Ability to travel at least 60% of the time (international and domestic) and possess a valid driver’s license.

What ICON can offer you

• Various annual leave entitlements.
• A range of health insurance offerings to suit you and your family’s needs.
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, LifeWorks, offering 24‑hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well‑being.
• Life assurance.
• Flexible country‑specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here.