Clinical Quality Manager

at  PAINCARE CENTER PTE LTD

Singapore, Southeast, Singapore -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate21 Jul, 2024USD 5000 Monthly28 Apr, 2024N/APatient Care,Service RecoveryNoNo
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Description:

JOB DESCRIPTION:

  • Extensive knowledge of Nursing acquired through significant experience in a Senior Clinical role.
  • Demonstrable experience in quality, safety, and operational leadership with a clear focus on the development and sustainability of services from a quality, outcomes and experience perspective with a clear drive and passion for service change, quality improvement, delivery, and transformation.
  • Experience of meeting regulatory compliance standards and the provision, maintenance, and reporting of data to meet compliance.
  • Demonstrable experience of the ability to work autonomously, initiating and organizing workloads, delegating appropriately, responding to changing priorities and meeting tight deadlines.
  • Demonstrable experience of the ability to make difficult decisions autonomously.
  • Demonstrable experience in preparing and delivering Training to enable others to achieve quality and compliance standards across the company.
  • Establish new and revise existing quality procedures and tools in support of audit and compliance activities.
  • Identify quality process and system improvements and implement timely actions.
  • Assist the clinical development organization in establishing procedures to support a risk-based approach to oversight of clinical trials using principles of quality by design and quality risk management.
  • Collaborate with key stakeholders in the development and implementation of comprehensive internal (systems and procedures) and external (investigator sites and vendors) audit programs and plans.
  • Serve as a quality subject matter expert and provide guidance to development personnel performing investigations, root cause analysis, and capas through knowledge of quality concepts and techniques.
  • Participate on cross-functional teams as subject matter expert in GCP/GLP/GVP to provide guidance and risk-based options that promote compliance.
  • Identify and communicate quality and compliance risks and participate in determination of appropriate planning to resolve and address issues and risks.
  • Lead the strategy and activities in support of health authority GCP/GLP/GVP inspections.
  • Review clinical study documents and check for consistency and compliance with relevant regulations, standards, and best practices.
  • Coordinate projects to successfully meet timelines.

Responsibilities:

Please refer the Job description for details


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Pharmaceuticals

Pharma / Biotech / Healthcare / Medical / R&D

Clinical Pharmacy

Graduate

Proficient

1

Singapore, Singapore