Clinical Research Manager - Toa Payoh

apartmentICON SOC Pte Ltd placeToa Payoh scheduleFull-time calendar_month 

This role is responsible for the operational oversight and management of the research portfolio and research team members.

Key responsibilities encompass financial oversight, staff leadership, investigator engagement, and business development, with a strong focus on aligning operations with Icon Cancer Centres to seamlessly integrate research into patient care. The role will report to the Global Operations Manager and will ensure that all clinical research is managed according to the International Council for Harmonization Guideline for Good Clinical Practice (GCP) and the relevant research protocol, thus ensuring the safety and protection of research participants and the reliability of research data.

Job Descriptions:

  • Manage feasibility and review of new research in collaboration with Investigators and other members of research leadership team.
  • Communicate effectively, professionally and respectfully with all internal and external stakeholders.
  • Evaluate performance and implement continuous process improvement practices.
  • Contribute significantly to the development and execution of Corrective and Preventive Action (CAPA) plans, including conducting root cause analyses to address issues and drive continuous improvement, liaise with vendors to address any concerns about quality and ensure data reliability.
  • Ensure all research is coordinated to a high standard as per the relevant protocol, local, and international standards including GCP.
  • Ensure compliance with Icon Research Standard Operating Procedures (SOPs), and Icon Group policies & procedures.
  • Monitor compliance with internal SOPs, regulatory requirements and reporting of protocol breaches or serious events.
  • Contribute to the development of policies and procedures within Icon Research and the organisation more broadly.
  • Promote a positive, team-oriented work environment.
  • Undertake additional responsibilities as directed by the manager in alignment with the role.

Job Requirements:

  • Relevant tertiary qualification in science, health, clinical research, or a related field, or equivalent demonstrated experience in a clinical research, healthcare, or scientific role
  • Minimum three years of experience as a Clinical Research Coordinator in the Clinical Haematology / Medical Oncology and/or Radiation Oncology/ Nuclear Medicine fields (s), including two years in a leadership role
  • Proven working knowledge of GCP and an understanding of regulatory and research governance requirements
  • Proven skills in negotiation, stakeholder management and influence
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