Study Start Up Associate II (Regulatory Submissions) Apply at locations: Chile, Santiago; Colombia, Bogota.
Time type: Full time. Posted on: Posted 3 Days Ago. Time left to apply: End Date: December 31, 2024 (30+ days left to apply). Job requisition id: JR123235.
Study Start Up Associate II (Regulatory Submissions) - Chile - Hybrid Scheme
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
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.
The Role As a Senior Study Start Up Associate at ICON, you'll work within a large-scale, fast-paced environment assisting the Study Start Up Team Lead in the development of the plan for country and site distribution and execution of SSU activities in assigned countries.
Responsible for performing feasibility, site identification, site contract negotiation, and other SSU activities. Provide country specific SSU expertise to Study Start Up team leads and project teams. Responsible for the preparation and coordination of submissions to regulatory, ethics, and other bodies. Develop, finalize, and review Master and Country Specific Subject Information Sheets/Informed Consent Forms. What you need: A Bachelor's Degree or local equivalent and/or appropriate experience from the Medical/science background and/or discipline. A minimum of 2 years of experience or understanding of clinical study start up requirements and activities. Strong understanding of regulatory requirements and guidelines for clinical trials, including ICH-GCP and local regulatory requirements. Excellent organizational and project management skills, with the ability to prioritize and manage multiple tasks simultaneously. Fluency in the local language and English is essential. 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 a range of health-related benefits to employees and their families. Our annual bonuses reflect delivery of performance goals – both ours and yours.
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 you need a reasonable accommodation for any part of the application process, please let us know.
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless.
About Us We want to be the Clinical Research Organisation that drives more client projects to market or accelerated decision than anyone else in the industry. If you're as driven as we are, join us. You'll be working in a great environment, with some of the brightest and the friendliest people in the sector.
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