Clinical Start-Up Program Manager

Premier Research Group

Singapore

Presencial

SGD 120 000 - 170 000

Tempo integral

há 8 horas
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Resumo da oferta

Premier Research Group is seeking a Manager, Start Up to join the Clinical Monitoring, Site Management and SSU team in Singapore. You will drive study start-up activities and lead staffing and resources to ensure timely delivery, while mentoring staff and maintaining compliance with SOPs and regulations.

The role requires strong project management, regulatory knowledge, and experience in CRO/pharma environments, with a focus on delivering high-quality start-up processes for life-changing

Qualificações

  • Undergrad degree in clinical/health-related field or equivalent.
  • Licensed health-care professional (e.g. RN) or equivalent experience.
  • Minimum 5 years in clinical research.
  • At least 2 years of people management experience.
  • Experience with CRO, device and/or pharmaceutical settings preferred.
  • Familiarity with FDA/EC regulations and ICH/GCP guidelines.
  • Knowledge of local health systems and cultural practices.

Responsabilidades

  • Manages staffing and resources to maximize department utilization.
  • Drives study start-up teams to meet timelines.
  • Identifies efficiencies to streamline start-up processes without compromising quality.
  • Mentors direct reports on HR, training and performance.
  • Maintains metrics and provides monthly updates to management.
  • Applies analytic skills to feasibility studies in planning stage.
  • Ensures staff stay current with SOPs and regulatory guidelines.
  • Establishes harmonized processes for start-up, maintenance and close-out.

Conhecimentos

People management
Project management
Regulatory knowledge
Analytical skills

Formação académica

Undergraduate degree in clinical/health-related field
Licensed healthcare professional (e.g. RN)

Descrição da oferta de emprego

Premier Research Group is seeking a Manager, Start Up to join the Clinical Monitoring, Site Management and SSU team in Singapore. You will drive study start-up activities and lead staffing and resources to ensure timely delivery, while mentoring staff and maintaining compliance with SOPs and regulations.

The role requires strong project management, regulatory knowledge, and experience in CRO/pharma environments, with a focus on delivering high-quality start-up processes for life-changing

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