Remote Clinical Research Associate

hace 1 día

Desde casa, México ICON A tiempo completo

**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 fulfill 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.**The Remote Clinical Research 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 but are not limited to identifying, training/initiating, and closing out 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.**The role**:- Ability to work on study teams that are often virtual, multi-cultural, and multi-disciplinary.- Serves as the primary contact for sites and investigators participating in studies.- Maintains, reviews, and ensures adequacy of information and data contained in site management reports, tracking systems (CTMS or others), and other site management documents.- Conducts and completes remote site management activities, with support as needed, according to applicable SOPs and the Site Management Plan.- Reviews drug storage and drug accountability procedures (as applicable), in accordance with applicable SOPs.- Assists with timely preparation and submission of regulatory documents for IRB/IEC submissions according to local requirements, with support, as needed.- Ability and willingness to travel as needed (drive and fly) - approximately 25% of the time.**Qualifications**:- 1+ year of clinical monitoring experience (on-site or remote)- Excellent written and oral communication in English- Working knowledge of MS office**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 fulfill your sense of purpose and drive lasting change.**_ #LI-Remote_**:**_ #LI-ND1_**:

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