Site Activation Specialist
5 days ago
Job Overview Under moderate supervision, executes the feasibility, site identificationregulatory, start-up, and maintenance activities in accordance withregulations, SOPs, and project requirements at the regional, or country level. Prepares and manages site documentation; reviews and negotiates site documents and contracts with sites and sponsors; maintains, reviews, and reports on site performance metrics; serves as the primary point of contact for investigative sites; tracks completion of appropriate documents for sites; ensures contracts are fully executed; and establishes project timelines. With moderate oversight and supervision, perform tasks at a country/region level associated with site activation activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities. Essential Functions With moderate oversight and supervision, serve a Single Point of Contact (SPOC) to perform feasibility, site activation and some maintenance activities in assigned studies for investigative sites, according to applicable regulations, SOPs and work instructions, working closely with the Site Activation Manager (SAM), Project Management team, and other departments as necessary. Review documents for completeness, consistency and accuracy, under guidance of senior staff. Prepare site documents, reviewing for completeness and accuracy. Inform team members of completion of regulatory contractual. and other documents for individual sites. Distribute completed documents to sites and internal project team members. Update and maintain internal systems, databases, tracking tools, timelines and project plans with accurate and complete project specific information. Review, track and follow up the progress, the approval and execution of required documents such as questionnaires, CDAs, regulatory, ethics, Informed Consent Form (ICF) and Investigator Pack (IP) release documents. Requires advanced knowledge within a specific discipline typically gained through extensive work experience and/or education. Qualifications Bachelor's Degree Life sciences or a related field Req And Other 1 - 3 years’ clinical research or other relevant experience; or equivalent combination of education, training and experience. Req With 3 years’ experience in a healthcare environment or equivalent combination of education, training and experience. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at #J-18808-Ljbffr
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Site Activation Specialist – Clinical Trials
3 days ago
Kwai Tsing District, Hong Kong SAR China IQVIA Full timeA leading global provider of clinical research services, this company is seeking a Site Activation Specialist to manage site activation and regulatory activities. The successful candidate will handle documentation and serve as a key contact for investigative sites, requiring a Bachelor's in Life Sciences and related experience. This full-time position offers...
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Kwai Chung, Hong Kong SAR China TWN IQVIA RDS Taiwan Ltd. Full timeA leading clinical research organization in Hong Kong seeks a candidate for site activation and management role. Responsibilities include serving as the main contact for investigative sites, preparing site documents, and ensuring compliance with regulations. Candidates should possess a Bachelor's degree in Life Sciences along with 1-3 years of clinical...
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Telecom Site Leasing
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Back Office Specialist
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Registered Safety Officer
5 days ago
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