Site Management Associate

il y a 2 jours

Paris, France ICON Temps plein

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.

The Site Management Associate is responsible for managing, implementing and monitoring clinical studies, with support, in a team setting according to ICON SOPs, SSPs and all applicable rules and regulations.

**The responsibilities of this position include**:

- Identifying, training/initiating and closing out of study sites.
- Conducting remote site monitoring visits and/or targeted on-site visits as needed.
- Conducting remote site management activities.
- Managing study sites and the required protocols, amendments and/or deviations, assuring that data is reported accurately and timelines are maintained.
- Assists with timely preparation and submission of regulatory documents for IRB/IEC submissions according to local requirements, with support, as needed.
- Maintains Sponsor and patient confidentiality
- Actively participates in regular meetings with Project Managers
- Assists in development of site and patient enrolment strategies with project team; works to motivate sites to meet enrolment timelines.
- Developing knowledge of and compliance with local regulatory requirements.

**Requirements**:

- A Bachelor’s degree in the life sciences, expertise with regulatory guidelines and clinical terminology.
- Demonstrable strong site management experience.
- You will need to have fluent written and spoken French and English skills.
- We would also welcome some previous experience as a CRA or an In
- house CRA.

**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.

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