4 дня назад
HGR Specialist (Clinical Research)
Вакансия из Hirify Global, списка международных tech-компанийДля мэтча и отклика нужен Plus
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
HGR Specialist (Clinical Research) (Site Activation/Regulatory): Managing feasibility, site identification, regulatory start-up, documentation, contracts, and maintenance activities for clinical research sites in Shanghai with an accent on regulatory compliance, document accuracy, and site performance tracking. Focus on coordinating site activation timelines, reviewing and executing essential documents, and maintaining accurate project systems and databases.
Location: Shanghai, China
Company
provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.
What you will do
- Execute feasibility, site identification, regulatory start-up, and site maintenance activities for assigned clinical studies.
- Serve as the primary point of contact for investigative sites and coordinate with Site Activation Managers, Project Management, and other departments.
- Prepare, review, distribute, and track site regulatory, contractual, ethics, and study documents.
- Review and negotiate site documents and contracts with sites and sponsors, ensuring contracts are fully executed.
- Maintain project timelines, plans, databases, tracking tools, and site performance metrics.
Requirements
- Bachelor's degree in life sciences or a related field.
- 1–3 years of clinical research or relevant experience, or an equivalent combination of education, training, and experience.
- At least 3 years of experience in a healthcare environment or equivalent experience.
- Knowledge of applicable regulations, standard operating procedures, and project requirements.
- Ability to review documents for completeness, consistency, and accuracy and manage site activation activities with moderate supervision.
Culture & Benefits
- Work within a global clinical research and healthcare intelligence organization.
- Collaborate with site activation, project management, and cross-functional teams.
- Follow established regulatory requirements, SOPs, work instructions, and contractual guidelines.
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