Senior Clinical Associate

At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives.Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.That’s our vision. We’re driven by it. And we need talented people who share it.If you’re as driven as we are, join us. You’ll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry.POSITION SUMMARY:To be an integral part of the study team whilst acquiring clinical and corporate knowledge of clinical trial conduct. Provide administrative support to the Project Manager(s), Clinical Trial Manager(s) and/or sites, with emphasis on driving global inspection readiness.

JOB FUNCTIONS/RESPONSIBILITIES:

• Recognize, exemplify and adhere to ICON's values which center around our culture of accountability, integrity, partnership, collaboration and excellence in delivery.  
• As a member of staff, the employee is expected to embrace and contribute to our culture of process improvement  with  a  focus  on  streamlining  our  processes  adding  value  to  our  business  and  meeting client needs  
• This  is  a  developmental  role  which  requires  extensive  training.    An  ability  and  willingness  to  travel (drive and fly) as needed for this role and at least 60% of the time for future roles is required.  
• To acquire knowledge of ICH GCP, the conduct of clinical trials and governing regulations, relevant ICON SOPs, ICON internal tracking systems and client SOPs / client systems (when applicable) 
• To  assist  the  project  teams  with  the  set-up,  organization  and  maintenance  of  clinical  study documentation (e.g. Study Files, CRFs, etc.) and guidelines (as appropriate) including preparation for internal/external audits, final reconciliation and archival   
• To  assist  in  the  processing  of  Data  Collection  Forms  i.e.  log  in,  tracking,  quality  control  as appropriate for the study   
• To share responsibility in the quality control audits of clinical study documentation (e.g. Study Files, CRF Files, Monitoring Files, etc.) to ensure study files are inspection ready at all times 
• To  facilitate  and  coordinate  ordering/dispatching  and  tracking  of  trial  materials  (e.g.  CRFs,  diary cards, lab supplies, drug supplies, and study binders) as appropriate  
• To  assist  project  teams  with  trial  progress  tracking  by  updating  the  Clinical  Trial  Management systems, providing access to study/client systems (as appropriate) 

Benefits of Working in ICON:Our success depends on the quality of our people. That’s why we’ve made it a priority to build a culture that rewards high performance and nurtures talent.We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals – both ours and yours.We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans – and related benefits such as life assurance – so you can save and plan with confidence for the years ahead.But beyond the competitive salaries and comprehensive benefits, you’ll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.