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ICONIC

Regulatory Affairs Associate

ICON plc is a leading global contract research organization dedicated to accelerating drug development and improving patient outcomes.

ICON

Employee count: 5000+

South Korea only

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Regulatory Affairs Associate position at ICON, a global healthcare intelligence and clinical research organisation, based in Seoul, South Korea. As a Senior Study Start Up Associate, you will lead site start-up and activation tasks, ensure regulatory compliance, and safeguard patient welfare.

Requirements

  • Bachelor's degree or local equivalent and/or appropriate experience from the Medical/science background and/or discipline.
  • At least 3 years of experience or understanding of clinical regulatory Affairs requirements and activities such as IND Submission and CMC process professionals.
  • Fluency in the local language and English is essential, enabling you to effectively communicate and collaborate with international teams.

Benefits

  • 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

About the job

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Posted on

Job type

Full Time

Experience level

Location requirements

Hiring timezones

South Korea +/- 0 hours

About ICON

Learn more about ICON and their company culture.

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Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life. We are a global provider of consulting and outsourced development and commercialisation services to pharmaceutical, biotechnology, medical device, and government and public health organizations. We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost, and increasing quality. Our global team of experts has extensive experience in a broad range of therapeutic areas.

We are proud to have developed 18 of the world's top 20 best-selling drugs, showcasing our commitment to driving advancements in the healthcare sector. Our extensive portfolio of services includes early clinical and bioanalytical solutions, specialty laboratory solutions, cardiac safety solutions, and many more. Additionally, we emphasize patient-centric trial design and real-world data strategies to optimize recruitment and ensure the success of clinical trials. Through these innovations, ICON is not only enhancing clinical research methodologies but also transforming the overall experience for sponsors, patients, and healthcare providers alike.

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ICON

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