Study Start Up Associate II
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.
Impactful work. Meaningful careers. Quality rewards.
At ICON, our employees are our greatest strength. That’s why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is lead a global team, become a deep scientific or technical expert, work in-house with our customers or gain experience in a variety of different ICON functions, we will support you in realising your full potential. Learn more about Our Culture at ICON
Day in the life
Teaser label
Our PeopleContent type
BlogsPublish date
12/10/2025
Summary
Zhong Yao's Journey at ICON Plc in China Zhong Yao's career in clinical research spans over two decades, with leadership roles across major CROs and a commitment to advancing healthcare in China.
Teaser label
IndustryContent type
BlogsPublish date
12/01/2025
Summary
How Data Moves Through a Clinical Trial Clinical research depends on one essential element: trustworthy data. Every safety decision, every statistical conclusion and every regulatory submission i
Teaser label
IndustryContent type
BlogsPublish date
11/28/2025
Summary
Quality and Compliance for New Entrants: A Plain Language Guide Quality and compliance can feel like dense subjects when you are entering clinical research for the first time. Many job
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