Informed Consent Specialist II

As an Informed Consent Specialist II, you will be responsible for the development, review, and approval of informed consent forms and supporting documents for clinical trials. Your primary duties will include: - Developing and reviewing informed consent forms and supporting documents to ensure compliance with applicable regulations, guidelines, and company standards - Collaborating with clinical trial teams, ethics committees, and regulatory authorities to obtain necessary approvals for informed consent forms - Providing training and guidance to clinical trial teams on informed consent procedures and requirements - Maintaining detailed documentation and records related to the informed consent process - Staying up-to-date with changes in regulations, guidelines, and industry best practices related to informed consent - Providing support and assistance to the Clinical Operations team as needed

ICON plc is a global provider of outsourced drug and device development and commercialisation services to pharmaceutical, biotechnology, medical device and government and public health organisations. We help our colleagues build exciting and rewarding careers and deliver results to help bring life-changing medicine and devices to market.