Project 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 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.
Overview:
Project Associate: Medical Affairs
Who are you?
You are a hard worker who thrives in a fast-paced environment. Your attention to detail and organizational skills has won you praise and you are regularly commended for meeting and beating deadlines. You look to make improvements - not accepting the status quo, but actively identifying issues that might put a project or deliverable at risk. You proactively look to do more and learn more
In this next step on your journey, you want to put your competitive, driven nature to work in an environment in which you can sharpen your business acumen, learn the CRO industry from the inside out, gain visibility and recognition. Additionally, you want to work for a company that both supports your professional growth and helps you find a work/life balance that lets you pursue your career passion and still be you. Most of all, you want to do it in a place where you're part of a team of experts as zealous about their work as you are.
You are a Project Associate
**Responsibilities**:
As a Project Associate, you are a key member of the Medical Affairs team, organizing project team and client meetings, as well as study information and materials. You are responsible for taking meeting minutes on global calls, filing in ETMF systems and training working closely with our global Medical Affairs team.
- Organizes meeting materials, binders, agendas and taking meeting minutes.
- Generates and maintains organizational charts, team calendar, newsletters, mass mailings, project specific information including but not limited to process flow charts, contact lists, holiday lists, study website, mailing labels.
- May support preparation of study files by maintaining and distributing project documents. Ensures documents within the electronic trial master file comply with filing/naming guidelines and have the correct status.
- Administrative Work
Qualifications:
You will need:
- Bachelor´s degree or international equivalent in business, finance, health sciences or related field
- 1, or 2 years' experience in clinical project administration or other relevant experience
- CRO, pharmaceutical or clinical research experience, preferred
- Advanced exp in the Office Package
- Intermediate Excel and Outlook
- Advanced English for Reading / Writing and Speaking
LI-AR2
LI-Onsite
Benefits of Working in ICON:
Our success depends on the knowledge, capabilities and quality of our people. That's why we are committed to developing our employees in a continuous learning culture - one where we challenge you with engaging work and where every experience adds to your professional development.
At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.
ICON, including subsidiaries, 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.

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