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Study Start Up Associate II

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About the role

This vacancy has now expired. Please see similar roles below...

 
"At ICON, it's our People that set us Apart"
 
ICON plc is a global provider of drug development solutions and services to the pharmaceutical, biotechnology and medical device industries. The company specialises in the strategic development, management and analysis of programs that support clinical development - from compound selection to Phase I-IV clinical studies. With headquarters in Dublin, Ireland, ICON currently, operates from 83 locations in 38 countries and has approximately 12,600 employees. Further information is available atwww.iconplc.com
 
This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. Working within a highly qualified team our Study Start up Associates coordinate clinical trial start-up activities and serve as primary contact for investigators and research coordinators in corporate and public sponsored human clinical trials for clinical studies in phases II – IV ensuring adherence to applicable regulations and principles of ICH-GCP.
 
 
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 1 year 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 pressurised environment.
 
 
What’s next?
 
Following your application you will be contacted by one of our dedicated recruiters and if successful we will be able to provide you with more details about this opportunity.
 
 
ICON is an equal opportunity employer - Minorities/Females/Disabled/Veterans and committed to providing a workplace free of any discrimination or harassment.
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