21 день назад
Site Activation Specialist (Contract)
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 (Contract) (Clinical Research): Managing feasibility, site identification, regulatory start-up, documentation, and maintenance activities for investigative sites in Seoul with an accent on regulatory compliance, document accuracy, and site performance tracking. Focus on coordinating IRB submissions, reviewing and negotiating site contracts, monitoring approval and execution timelines, and maintaining study databases and project plans.
Location: Seoul, Republic of Korea
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 maintenance activities for assigned clinical studies.
- Act as the primary point of contact for investigative sites and coordinate with Site Activation, Project Management, and other departments.
- Prepare, review, distribute, and track regulatory, contractual, ethics, informed consent, and investigator documentation.
- Follow up on document approvals, execution, and completion, including questionnaires and confidentiality agreements.
- Maintain study databases, tracking tools, timelines, project plans, and site performance metrics.
- Support site document and contract review and negotiation with sites and sponsors.
Requirements
- Bachelor's degree in life sciences or a related field.
- Experience in regulatory start-up, clinical research associate, or study coordinator roles.
- Experience with initial and maintenance IRB submissions.
- Good English communication skills required.
- Ability to review documents for completeness, consistency, and accuracy under guidance of senior staff.
- One-year contract position based in Seoul, Republic of Korea.
Nice to have
- Exposure to site budget and contract negotiation activities.
- Strong clinical research experience and willingness to develop in site start-up and maintenance activities.
Culture & Benefits
- Work on clinical research projects supporting the development of medical treatments and improved patient outcomes.
- Collaborate with regional and country-level study teams and investigative sites.
- Operate according to applicable regulations, standard operating procedures, project requirements, and contractual guidelines.
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