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ICON plc

Clinical Data Risk Analyst - Mandarin speaker

Posted 16 Days Ago
Be an Early Applicant
In-Office
Dublin, IRL
Entry level
In-Office
Dublin, IRL
Entry level
Conduct clinical trial data risk assessments, identify data integrity issues, recommend mitigation strategies, and monitor data quality throughout trials. Collaborate with cross-functional teams on risk management plans, communicate statistical insights using analysis and visualization tools, and support regulatory documentation and audit preparation. The role requires clinical research or data analysis experience, strong analytical skills, English and Mandarin fluency, and knowledge of statistical and risk assessment methodologies.
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Clinical Data Risk Analyst

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.


As a Clinical Data Risk Analyst (Speaking Mandarin) at ICON, you will identify and mitigating risks associated with clinical trial data. You will contribute to the overall success of our clinical programs by employing risk assessment methodologies to ensure data integrity and compliance with regulatory standards.


What You Will Do:


Your role will involve delivering clinical research work to a high standard, working closely with your team and stakeholders.

Key responsibilities include:

  • Conducting risk assessments on clinical trial data to identify potential issues and recommend mitigation strategies.
  • Collaborating with cross-functional teams to develop and implement risk management plans and protocols.
  • Monitoring data quality and integrity throughout the trial process, reporting findings to stakeholders.
  • Utilizing statistical analysis and visualization tools to communicate risk-related insights effectively.
  • Supporting the preparation of risk management documentation for regulatory submissions and audits.

Your Profile:


You will bring relevant clinical research experience, along with the following qualifications and skills.

Required qualifications and experience:

  • Degree in statistics, life sciences, or a related field.
  • Proficiency in English and Mandarin mandatory.
  • Experience in clinical data analysis or risk management within a clinical research environment.
  • Strong analytical skills with proficiency in statistical software and risk assessment methodologies.
  • Attention to detail and a proactive approach to identifying and addressing data risks.
  • Effective communication skills, with the ability to collaborate across diverse teams and convey complex information clearly.

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

HQ

ICON plc Dublin, Dublin, IRL Office

ICON plc, South County Business Park, Dublin, Ireland

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