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Study Start Up Associate II

JR061562

About the role

This vacancy has now expired. Please click here to view live vacancies.

Study Start Up Associate II role within ICON:

Key responsibilities:

  • Prepare, review contract negotiation with external sites in China, working to project deadline to finalise study contracts
  • You will be collaborating with multiple internal and external teams to coordinate the contract templates and budgets throughout the timeframe
  • Completing contract amendment activities

Other study start up activities as required including: ethics submissions, creating submissions packages, amendments to study documentation according to country guidelines in China

To succeed you will need:

  • Bachelor's Degree preferably in life sciences will ensure your familiarity with regulatory guidelines and industry knowledge.
  • Minimum of 2 years of experience or understanding of clinical study start up requirements and activities.
  • Fluent in local language and English, you will possess excellent written and verbal communication and interpersonal skills enabling you to deal with queries in a timely manner.
  • You should be able to produce accurate work to tight deadlines within a pressurized environment.
List #1

Day in the life

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Driving Trials Forward: Study Start-Up Leadership at ICON

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Publish date

03/16/2026

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Driving Study Start-Up: James Pereira's Journey at ICON James Pereira's career in clinical research has been shaped by a single driving question: how do we get studies started faster? From his earl

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Explore James Pereira's career in study start-up at ICON, leading global teams to accelerate patient access.

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Who’s Who in a Clinical Trial Team

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Publish date

03/15/2026

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Who's Who In a Clinical Trial Team Clinical trials rely on large, cross functional teams working together across countries, time zones and specialisms. For those new to the industry, the number of

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Understand the key roles in a clinical trial team, from study start up and site activation to data, safety and quality.

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Learn how clinical trials are delivered by understanding the roles of sponsors, CROs, and sites.

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