Locations possible : Bulgaria (Sofia), Serbia (Belgrade), Poland (Warsaw)
Office-based or Home-Based
This role is open to current or former Clinical Research Associates
or professional with clinical trial experience
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.
Job Description :
• Assist the relevant operational staff in the development and implementation of clinical quality plans at the department and study level.
• Assist with monitoring assessment of quality metrics and/or key quality indicators.
• Identify potential non compliance/breaks of quality control steps taken by operations as measured thru SOP, WP and industry standards
• Escalation as appropriate to senior management with proposed solutions
• Review of deliverables in conjunction with issues that are affecting the quality of the clinical deliverables to ensure quality standards are achieved.
• Prepare reports of trends in Clinical QC findings for management.
• Assist in the development of corrective and preventative action plans for the department when required.
• Train new Clinical Quality Compliance staff on processes and procedures.
• Provide QC services to other operational departments/vendors, as required.
• Scheduling and managing internal and external meetings, assisting in the production of presentation materials, generating meeting minutes.
• Contacting external and internal individuals to collate relevant study information.
Requirements :
Relevant experience as a Sr.CRA / Lead CRA / Quality Auditor
Strong understanding on Clinical Quality Compliance processes
Excellent communication skills
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.
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