3 дня назад
Site Activation 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
Site Activation Specialist (Clinical Research): Managing feasibility, site identification, regulatory start-up, documentation, and maintenance activities for clinical research sites in Singapore with an accent on regulatory compliance, contract execution, and accurate project tracking. Focus on coordinating investigative sites, reviewing and negotiating essential documents, monitoring site performance, and maintaining activation timelines and databases.
Location: Singapore
Employment: Full time, 7-month contract
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, activation, and selected 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 documentation for completeness, consistency, accuracy, approval, and execution.
- Review and follow up on questionnaires, confidentiality agreements, regulatory and ethics documents, informed consent forms, and Investigator Pack release documents.
- Maintain project databases, tracking tools, timelines, plans, and site performance metrics.
- Establish project timelines and confirm completion of contractual, regulatory, and other required site documents.
Requirements
- Bachelor's degree in life sciences or a related field.
- 1–3 years of clinical research or other relevant experience, or an equivalent combination of education, training, and experience.
- 3 years of experience in a healthcare environment, or an equivalent combination of education, training, and experience.
- Knowledge of applicable regulations, standard operating procedures, work instructions, and project requirements.
- Ability to review documents and maintain accurate project-specific information under 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 structured regulatory, quality, and operating procedures.
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