Study Start Up Associate I
About the role
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Study Start Up Associate I
Location: Taipei
At ICON, it's our people that set us apart.
As a global provider of drug development solutions, our work is serious business. As a member of the Study Start Up Team, you will play an integral role in making sure that physicians at our research sites are prepared to start the trial of investigational, new pharmaceutical and biological products for clinical trials at their local practices.
Key responsibilities:
Prepare, review contract negotiation with external sites, working to project deadline to finalise study contracts
To be familiar with ICH GCP, relevant country regulations /guidelines and ICON SOPs
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
To undertake other reasonably related duties as may be assigned from time to time
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' demonstrated experience of clinical study start up requirements and activities from regulatory submissions preferably contract/budget negotiations
Possess excellent written and verbal communication and interpersonal skills enabling you to deal with queries in a timely manner
You should be able to work autonomously, produce accurate work to tight deadlines within a pressurised environment
OUR OFFERINGS TO YOU
Here at ICON we believe in growing your career with us, providing you access to a world class learning platform, training programs to upgrade your skills not only professionally but personally. If you have the desire to grow in management, we have a fantastic management program, your managers will also prepare you along the way as you step up in your career and guide you towards your goal. The opportunity to excel in your career is yours to own and it can either be with ICON Core team or in our FSP/insourcing model.
LOOK NO FURTHER! Submit your application now and be part of our ICON family, an award winning Global CRO!
#LI-CK1
#LI-APAC2
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
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Our PeopleContent type
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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.
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12/01/2025
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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
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11/28/2025
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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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