ICON plc Logo

ICON plc

Clinical Research Associate

Reposted 13 Days Ago
Be an Early Applicant
In-Office
Singapore, SGP
Junior
In-Office
Singapore, SGP
Junior
As a Clinical Research Associate, you will coordinate clinical trials, ensure regulatory compliance, and maintain study documentation, while establishing relationships with stakeholders.
The summary above was generated by AI
Evergreen Requisition: JR141278 Clinical Research Associate

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


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

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


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


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

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

Similar Jobs

18 Days Ago
In-Office
Singapore, SGP
Junior
Junior
Biotech
Manage clinical study sites, ensuring adherence to protocols and regulations. Conduct monitoring visits and maintain regulatory documents. Prepare reports and train new employees.
Top Skills: Clinical Trial Management System (Ctms)E-Clinical SystemsMicrosoft Office Applications
7 Days Ago
In-Office
Singapore, SGP
Senior level
Senior level
Healthtech • Biotech • Pharmaceutical • Manufacturing
As a Senior Clinical Research Associate, you will manage clinical trials, ensuring compliance with protocols and regulations, mentoring staff, and maintaining site relationships while overseeing multiple projects.
Top Skills: Clinical Trial SoftwareTools
21 Days Ago
In-Office
Singapore, SGP
Junior
Junior
Healthtech
As a Senior CRA, you will conduct site visits, monitor trial progress, manage documentation, communicate with stakeholders, and ensure compliance with clinical research regulations.
Top Skills: GCPMS Office

What you need to know about the Singapore Tech Scene

The digital revolution has driven a constant demand for tech professionals across industries like software development, data analytics and cybersecurity. In Singapore, one of the largest cities in Southeast Asia, the demand for tech talent is so high that the government continues to invest millions into programs designed to develop a talent pipeline directly from universities while also scaling efforts in pre-employment training and mid-career upskilling to expand and elevate its workforce.

Sign up now Access later

Create Free Account

Please log in or sign up to report this job.

Create Free Account