Clinical Research Associate

ICON Strategic Solutions; Singapore; On-site; SGD 60,000 - 80,000; Full time

Job summary

A global healthcare organization in Singapore is seeking a Clinical Research Associate II to oversee clinical trials and ensure regulatory compliance. The successful candidate will coordinate study activities, analyze data, and engage with stakeholders. Ideal candidates have a university degree in medicine or science, along with at least 2 years of monitoring experience. This role involves significant travel (up to 60%) and offers a competitive salary along with various employee benefits focused on well-being and work-life balance.

Benefits

Various annual leave entitlements

Health insurance offerings

Competitive retirement planning

Global Employee Assistance Programme

Life assurance

Flexible optional benefits

Qualifications

• At least 2 years of monitoring experience as a CRA.
• Knowledge of ICH-GCP guidelines and expertise to review medical data.
• Ability to travel at least 60% of the time.

Responsibilities

• Coordinate all activities for setting up and monitoring a study.
• Ensure patient safety by ensuring compliance with ICON’s procedures.
• Develop and maintain strong relationships with stakeholders.

Skills

Clinical trial oversight

Monitoring experience

Knowledge of ICH-GCP guidelines

Written and verbal communication in English

Social skills

Education

University degree in medicine, science, or equivalent

Job description

Clinical Research Associate II

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

We are currently seeking a Clinical Research Associate to join our diverse and dynamic team at ICON Plc. As a key member of our research department, you will be responsible for overseeing and coordinating clinical trials, ensuring compliance with regulations, and collecting and analyzing critical data.

What you will be doing

• Working independently and actively to coordinate all activities for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation
• Running sponsor generated queries efficiently and taking responsibility for study cost efficiency; you will also participate in the preparation and review of study documentation and feasibility studies for new proposals as required.
• Develop and maintain strong, collaborative relationships with key stakeholders, clinical investigators, and site staff.
• Ensure patient safety by ensuring compliance with ICON’s procedures, protocols, and regulatory requirements.

Your profile

• At least 2 years of monitoring experience as a CRA.
• University degree in medicine, science, or equivalent
• Knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data
• Excellent written and verbal communication in English
• Good social skills enabling you to deal with queries in a timely manner
• Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid drivers license

What ICON can offer you:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well‑being and work life balance opportunities for you and your family.

Our benefits examples include:

• 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.

Visit our careers site to read more about the benefits ICON offers.

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

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Are you a current ICON Employee? Please click here to apply