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5 дней назад

Manager, Start Up (Clinical Research)

Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
Singapore
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Manager, Start Up (Clinical Research): Managing study start-up teams, staffing, resources, and timelines for clinical research projects across multiple countries with an accent on process optimization, feasibility analysis, and regulatory compliance. Focus on coordinating direct reports, improving harmonized start-up processes, forecasting utilization, and supporting complex CRO, device, and pharmaceutical studies.

Location: Singapore

Company

hirify.global supports biotech, medtech, and specialty pharma companies in developing medicines, medical devices, and diagnostics through clinical research services.

What you will do

  • Manage study start-up teams, resources, staffing, and timelines across multiple countries.
  • Lead and mentor direct reports, including training, performance management, career development, and annual evaluations.
  • Improve and harmonize processes for study start-up, essential document maintenance, study maintenance, and closeout.
  • Analyze metrics, feasibility data, staffing forecasts, costing, and utilization to support study planning and cost efficiency.
  • Support proposals, business development, client presentations, stakeholder communication, and transition planning.
  • Ensure compliance with company SOPs, industry regulations, ICH/GCP requirements, and applicable regulatory procedures.

Requirements

  • Undergraduate degree or international equivalent in a clinical, scientific, or health-related field, a licensed healthcare qualification, or equivalent work experience.
  • At least 5 years of experience in the clinical research industry.
  • At least 2 years of people management experience.
  • Analytical skills for reviewing metrics and feasibility data, with knowledge of project management principles.
  • Working knowledge of ICH/GCP regulations, FDA and European regulatory procedures, and national or local health systems.
  • Fluent written and verbal English required; the role is based in Singapore.

Nice to have

  • Experience in a contract research organization, medical devices, or pharmaceuticals.
  • Knowledge of cultural and professional practices relevant to countries or regions where study start-up activities are conducted.

Culture & Benefits

  • Opportunities for professional growth, skills development, and career progression.
  • Flexible working practices intended to support work-life balance.
  • Participation in corporate initiatives and cross-functional knowledge sharing.
  • Work in a global environment coordinating studies across multiple countries.

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