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Korea Office/Remote Pharma Solutions Clinical Research Associate I/II

I

Location
South Korea
ICON

Job Description

Korea Office/Remote Pharma Solutions Clinical Research Associate I/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 I/II to join our diverse and dynamic team. As a Clinical Research Associate I/II at ICON, you will play a pivotal role in monitoring clinical trials, ensuring compliance with study protocols and regulatory requirements, and contributing to the advancement of innovative treatments and therapies through meticulous oversight and data collection.

What You Will Be Doing:

  • Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.

  • Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.

  • Collaborating with investigators and site staff to facilitate smooth study conduct.

  • Performing data review and resolution of queries to maintain high-quality clinical data.

  • Contributing 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 1 year of Oncology onsite monitoring CRA experience

  • Or 1 year of onsite monitoring CRA experience including Oncology CRC/SC experience

  • 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.

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, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised 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, subsidised travel passes, health assessments, among others.

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

ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, 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

Advice from our career coach

A successful applicant for the Clinical Research Associate I/II position at ICON should have a bachelor's degree in a scientific or healthcare-related field and a minimum of 1 year of Oncology onsite monitoring CRA experience or equivalent experience in clinical research. Knowledge of clinical trial processes, regulations, and ICH-GCP guidelines is essential, along with strong organizational and communication skills. To stand out as an applicant, consider the following tips:

  • Highlight your expertise in Oncology site monitoring or related experience in clinical research.
  • Showcase your knowledge of clinical trial processes and regulatory requirements.
  • Emphasize your attention to detail and ability to work independently and collaboratively in a fast-paced environment.
  • Demonstrate strong communication skills and the ability to work effectively with investigators and site staff.
  • Research ICON's culture and values to align your application with the company's mission and priorities.

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About the job

Oct 17, 2024

Full-time

  1. KR South Korea
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