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Clinical Research Associate - Singapore  

Company managed [?] Still accepting applications

Posted on : 09 May 2017

Project Description

Description:
  • Our company  is the leading global provider of outsourced clinical research services.  
  • Customers include the leading global pharmaceutical companies as well as a number of biotechnology and small to mid-sized pharmaceutical companies. 
  • Our focus is on the development of innovative pharmaceuticals with the goal of enabling companies to reach early decisions concerning which compounds to progress further into clinical development.
  • Our company provides these services through three clinical research units with over 600 beds located in the US and Europe. 
  • In addition, our company provides clinical research services through partnerships with other clinical research units in North America, Europe and Asia. 
  • Supporting our clinical work are two world class bio-analytical laboratories located in Europe and the US.
  • Our facility is looking for a Clinical Research Associate to join the team.
  • The Clinical Research Associate (CRA) will perform monitoring and investigator site management activities for clinical trials, clinical investigations and other interventional or non-interventional studies.



Primary Responsibilities: 
  • Clinical monitoring and site management for clinical studies of phases I-IV 
  • Regulatory activities with authorities, ethics committees and investigators 
  • Project management support and in-house activities for clinical research projects 
  • Sponsor communication and contact 



Knowledge/Skills/Education/Licenses:  
  • Bachelor's degree in biomedical-related field, life sciences or equivalent field. 
  • Two years working experience in clinical research, as a CRA, Study Nurse or related profession preferred. 
  • One year experience in on-site monitoring preferred. 
  • Excellent oral and written communication skills in English and the other official languages of Singapore.
  • Knowledge of other languages advantageous. 
  • High level of organization, multi-tasking, judgement, and keeping to timelines. 
  • Profound knowledge of ICH-GCP and other relevant regulatory requirements. 
  • Flexible and willing to travel up to 70%. 
  • Ability to anticipate and prevent problems and also create backup plans.   
  • Equivalent education and experience will be considered.