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台灣愛康恩招募臨床試驗法規專員(Study Start-up Associate)、臨床試驗研究專員(Clinical Research Associate) 數名

ICON - A Symbol of Excellence

 "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 at www.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.

 

Benefits of Working in ICON

Other than working with a great team of smart and energetic people, we also offer a very competitive benefits package.  This varies from country to country so a dedicated recruiter will discuss this with you at interview stage.

We care about our people as they are the key to our success. We provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long term career. 

ICON is an equal opportunity employer - M/F/D/V and committed to providing a workplace free of any discrimination or harassment.

 

Contact information

Grace Lin Grace.lin@iconplc.com

 

【Job openings 1】

Clinical Trial Assistant - Entry level (Location: Taipei)

Key responsibilities:

  • Must demonstrate the ability to provide and receive constructive feedback, appreciate team goals, respect others point of view and seek advise when appropriate
  • Good organizational skills, ability to manage multiple task and meticulous attention to detail
  • Good written and verbal communication skills in local language and English
  • Computer literacy: e.g. Microsoft Word, Excel, PowerPoint, Outlook
  • You will be collaborating with multiple internal and external teams across different countries and regions. Must possess the ability to work on study teams which are often virtual, multi-cultural and multi-disciplinary.

To succeed you will need:

Bachelor’s Degree preferably in life sciences or local equivalent

 

【Job openings 2】

Study Start Up Associate (SSUA) - All levels (Location: Taipei)

Key responsibilities:

  • Prepare, review contract negotiation with external sites in Taiwan, 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 Taiwan

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.

 

【Job openings 3】

Clinical Research Associate (CRA) - All levels (Location: Taipei)

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 Clinical Research Associates (CRA’s) identify, select, initiate and close-out investigational sites for clinical studies in phases II – IV ensuring adherence to applicable regulations and principles of ICH-GCP.

Overview of the Role

  • Working independently and proactively to coordinate all necessary activities required for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation.  You will be involved in the submission of protocol, consent documents for ethics/IRB approval and assist in the preparation of regulatory submissions as requested
  • Managing sponsor generated queries efficiently and taking responsibility for study cost effectiveness; you will also participate in the preparation and review of study documentation and feasibility studies for new proposals as required.  
  • Depending on your level of experience, you may assist in training and mentoring less experienced CRA’s and/or manage CRA’s working on international projects 

Role Requirements 

  • With a University degree in medicine, science, or equivalent; ideally you will have a minimum of 6 months previous monitoring experience in medium sized studies, including study start-up and close-out (for all roles above Entry Level).  You should also have knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data
  • 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  
  • You will have the opportunity to progress your career and may wish to move into Project Management or into other related areas where you can further develop your skill set.  
  • Percentage of travel will vary up to 60%

 

 



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