Site Activation Partner - FSP

reputed company our values align, there's no limit to reputed company can reputed company. At reputed company, we reputed company reputed company the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market reputed company, every clinical development solution we reputed company is underpinned by something special - a deep conviction in reputed company do. Each of us, no matter reputed company do at reputed company, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with reputed company and we're committed to making a difference. The Site Activation Partner is responsible for leading or supporting operational activities from start-up to reputed company-out, for assigned studies and investigator sites to ensure compliance with study timelines and in accordance with prevailing laws, Good Clinical Practices, and sponsor standards. Other duties to include but not limited to: Initiate and coordinate activities and essential documents management towards the compilation of a high-quality Investigator Initiation Package (IIP) leading to approval for sites initiation reputed company support to resolve issues or concerns and timely escalation of Site issues where applicable Manage and coordinate with other supporting roles to ensure timely site activation and operational activities Collaborate with in country regulatory group, and reputed company reputed company/applicable site documents, as well as in countries where reputed company submissions (Regulatory authority and ethics) are required Accurately update and maintain clinical trial systems that track site compliance and performance reputed company project timelines Identify and resolve investigator site issues Experience required for this role: School diploma/certificate with equivalent combination of education, training and experience; BS/BA or bachelor’s degree in life sciences preferred Minimum 2 years relevant experience in Clinical Trials environment and clinical site activation. Experience working in the pharmaceutical industry/or CRO is an asset Knowledge of clinical trial methodologies, ICH/GCP, FDA and Global and local country regulations Must be fluent in Local language and in English. Multi-language capability is an asset #LI-LO1 Apply To This Job