Study Start Up Specialist II （FSP）

Coordinate guide and assist with all start up activities prior to site activation, including but not limited to: Site Informed Consent Form (ICF) localization and guidance in line with regulatory/health authority requirements.

Maintain up to date knowledge, ensure adherence and compliance with local regulatory

requirements and associated documentation.

QualificationsUniversity Degree or Equivalent preferably in a medical/science-related field.

Prior work experience demonstrating knowledge and understanding of clinical trials, such as that obtained in a clinical trial monitor capacity, and experience managing projects.

Demonstrated knowledge and understanding of ICH-GCP, the regulatory, ethics and contractual requirements for starting clinical trials in relevant country.