Job Description
Clinical Trial Submission Manager Associate
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.
We are currently seeking a Regulatory Affairs Specialist to join our diverse and dynamic team. As a Regulatory Affairs Specialist at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.
**What you will be doing**
+ Notification to ECs and RA, Post activities management
+ Amendment submission to ECs and RA. This will include submission via RA portal.
+ EC submission: printing & shipping of the dossiers (initial, amendments and notifications) for ECs requiring pa...
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.
We are currently seeking a Regulatory Affairs Specialist to join our diverse and dynamic team. As a Regulatory Affairs Specialist at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.
**What you will be doing**
+ Notification to ECs and RA, Post activities management
+ Amendment submission to ECs and RA. This will include submission via RA portal.
+ EC submission: printing & shipping of the dossiers (initial, amendments and notifications) for ECs requiring pa...
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