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6 часов Π½Π°Π·Π°Π΄

Site Activation Specialist (SSU/RSU)

Π€ΠΎΡ€ΠΌΠ°Ρ‚ Ρ€Π°Π±ΠΎΡ‚Ρ‹
onsite
Π’ΠΈΠΏ Ρ€Π°Π±ΠΎΡ‚Ρ‹
fulltime
Π“Ρ€Π΅ΠΉΠ΄
middle
Английский
b2
Π‘Ρ‚Ρ€Π°Π½Π°
Taiwan
Вакансия ΠΈΠ· списка Hirify.GlobalВакансия ΠΈΠ· Hirify Global, списка ΠΌΠ΅ΠΆΠ΄ΡƒΠ½Π°Ρ€ΠΎΠ΄Π½Ρ‹Ρ… tech-ΠΊΠΎΠΌΠΏΠ°Π½ΠΈΠΉ
Для мэтча ΠΈ ΠΎΡ‚ΠΊΠ»ΠΈΠΊΠ° Π½ΡƒΠΆΠ΅Π½ Plus

ΠœΡΡ‚Ρ‡ & Π‘ΠΎΠΏΡ€ΠΎΠ²ΠΎΠ΄

Для мэтча с этой вакансиСй Π½ΡƒΠΆΠ΅Π½ Plus

ОписаниС вакансии

ВСкст:
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TL;DR
Site Activation Specialist (SSU/RSU) (Clinical Research): Managing country-level site activation and regulatory document workflows for clinical studies with an accent on site readiness, compliance, and project timelines. Focus on coordinating investigative sites and project teams, tracking ethics and regulatory approvals, and maintaining accurate clinical systems and quality-controlled documentation.

Location: Taipei, Taipei City, Taiwan

Company

hirify.global provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

  • Act as the single point of contact for investigative sites, Site Activation Managers, project management, and internal departments.
  • Perform country-level start-up and site activation activities in line with regulations, SOPs, work instructions, project requirements, and timelines.
  • Prepare, distribute, review, track, and follow up on regulatory, ethics, contractual, informed consent, and investigator package documents.
  • Maintain project information in internal systems, databases, and tracking tools.
  • Review site performance metrics, provide feedback to management, and support project planning and contingency measures.
  • Perform quality control of site documents and provide local expertise to project teams and sponsors when required.

Requirements

  • Bachelor’s degree in life sciences or a related field, with at least 3 years of clinical research or relevant experience, or an equivalent combination of education, training, and experience.
  • At least 3 years of clinical research experience, including 1 year in a leadership capacity.
  • In-depth knowledge of clinical systems, procedures, corporate standards, and the regulated clinical trial environment.
  • Knowledge of GCP/ICH and applicable local regulatory requirements, SOPs, and company standards.
  • Strong communication, negotiation, organizational, interpersonal, and prioritization skills.
  • Ability to work independently, manage multiple projects, and maintain effective relationships with coworkers, managers, clients, and sponsors.

Culture & Benefits

  • Work is performed within a global clinical research and healthcare intelligence organization.
  • Responsibilities follow defined regulatory, quality, SOP, and project governance standards.
  • Collaboration includes investigative sites, project teams, managers, clients, and sponsors.

Π‘ΡƒΠ΄ΡŒΡ‚Π΅ остороТны: Ссли Ρ€Π°Π±ΠΎΡ‚ΠΎΠ΄Π°Ρ‚Π΅Π»ΡŒ просит Π²ΠΎΠΉΡ‚ΠΈ Π² ΠΈΡ… систСму, ΠΈΡΠΏΠΎΠ»ΡŒΠ·ΡƒΡ iCloud/Google, ΠΏΡ€ΠΈΡΠ»Π°Ρ‚ΡŒ ΠΊΠΎΠ΄/ΠΏΠ°Ρ€ΠΎΠ»ΡŒ, Π·Π°ΠΏΡƒΡΡ‚ΠΈΡ‚ΡŒ ΠΊΠΎΠ΄/ПО, Π½Π΅ Π΄Π΅Π»Π°ΠΉΡ‚Π΅ этого - это мошСнники. ΠžΠ±ΡΠ·Π°Ρ‚Π΅Π»ΡŒΠ½ΠΎ ΠΆΠΌΠΈΡ‚Π΅ "ΠŸΠΎΠΆΠ°Π»ΠΎΠ²Π°Ρ‚ΡŒΡΡ" ΠΈΠ»ΠΈ ΠΏΠΈΡˆΠΈΡ‚Π΅ Π² ΠΏΠΎΠ΄Π΄Π΅Ρ€ΠΆΠΊΡƒ. ΠŸΠΎΠ΄Ρ€ΠΎΠ±Π½Π΅Π΅ Π² Π³Π°ΠΉΠ΄Π΅ β†’