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 friendliest people in the sector, and you'll be helping shape an industry.
We currently have an opportunity for a Client Services Associate I, a client facing role.
The Role Responsibilities:
- Draft and negotiate contract amendments.
- Follow up with sites with regard to the execution status of CTAs and process fully executed agreements per the governance plan.
- Follow-up with sites regarding documents needed to support timely and accurate payments including PICs, W-9s, and W-8s.
- Running and analyzing reports, identifying delays in the contract execution process, providing follow-up, and escalating appropriately in coordinating the completion of Clinical Trial Agreements.
- Schedule weekly reports for each assigned study and forward to the appropriate Contract Analyst as needed.
- Review reports for each assigned study to identify non-responsive sites, sponsors, and/or Contract Analysts as needed.
- Review reports for each assigned study to identify UPS, site, ICON, and/or sponsor delays in the signature process for final CTAs, Amendments and Ancillary Agreements.
- Communication support and administrative support to project teams.
- Demonstrates professionalism in conducting daily activities.
You will need:
- Bachelor's Degree preferred
- Read, write, and speak fluent English
- Proficient office/administrative skills
- Industry experience is not required
- Ability to manage time and pivot quickly with efficiency
- Excellent written, and oral communication, and presentation skills
- Proficient in Microsoft Office Suite Applications.
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.
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 organization: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organization 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.
As a Clinical Research Associate at ICON, you'll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to 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.
The role:
- Independent, proactive work to set up and monitor studies, complete reports and maintain documentation
- Submitting protocol, consent documents for ethics/IRB approval, as well as preparing regulatory submissions
- Balancing sponsor generat
