Clinical Project Manager

BH-226392
  • Competitive remuneration package
  • Australia New South Wales Sydney
  • Permanent
  • Life Sciences
Clinical Project Manager - CRO

  • Oncology & Cardiology focus
  • Flexible & remote working available
  • A truly collaborate research environment
  • Early phase studies
  • Competitive remuneration package
  • Career stability & job security
We are seeking an ambitious Clinical Project Manager for an opportunity to take on a key role within this deeply experienced and dynamic team.

The Clinical Project Manager is responsible for ensuring clinical research projects are properly resourced, managed, executed and reported within budget and in accordance with established timelines and quality standards.

The role
  • Manage the planning, implementation, ongoing evaluation, prioritisation, reporting of all operational aspects of allocated projects.
  • Act as the point of contact for assigned projects for sponsor and internal study teams.
  • Support research Business Development in the Request for Proposal (RFP) and Bid Defence processes; initial project plans, costings, drafting responses to RFPs and participating in client presentations.
  • Provide accurate input into standard contracts used in clinical research including Confidentiality Agreements, Letter of Intent, Indemnity Forms, Contracts for Service and Works Orders.
  • Provide guidance to the project team on deliverables.
  • Oversee the preparation of study essential documents; prepares protocol, amendments, CRF, informed consent form, operations.
  • Manage the day-to-day study operations, including management of vendors and coordination of activities.
  • Ensure the accurate and timely review and approval of monitoring reports.
  • Plan and implement Patient recruitment and retention strategies.
  • Prepare and manage the Study Budget for assigned studies.
  • Set up the project requirements in the Clinical Trial Management Systems.
  • Conduct and implement other activities such as writing of SOPs and Working Instructions.
You
  • A positive 'can do' attitude
  • Degree level qualification in Life Sciences (e.g., Biology, Chemistry, Pharmaceuticals)
  • Strong experience in clinical research in CRO, Pharma and/or Biotech industry, as a Project Manager
  • Proven track record of having successfully led complex global clinical trials
  • Experience across all functional capabilities involved in CRO-directed clinical research
  • Demonstrable experience in client interaction & vendor management
  • Comprehensive practical knowledge of ICH-GCP requirements, including across different jurisdictions
  • Understanding of clinical trial budgets, client and site contracts and client billing
  • Experience working in Oncology and Cardiology therapeutic areas highly preferable
  • Able to work in an international environment with internal & external team partners

To be considered here, please submit your CV or for any confidential questions in advance contact Nick Shearing on 0477 600 716 / (02) 9189 9084.

With over 90 years' combined experience, NES Fircroft (NES) is proud to be the world's leading engineering staffing provider spanning the Oil & Gas, Power & Renewables, Infrastructure, Life Sciences, Mining, Automotive and Chemicals sectors worldwide.With more than 100 offices in 45 countries, we are able to provide our clients with the engineering and technical expertise they need, wherever and whenever it is needed. We offer contractors far more than a traditional recruitment service, supporting with everything from securing visas and work permits, to providing market-leading benefits packages and accommodation, ensuring they are safely and compliantly able to support our clients.

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