Freelance Clinical Project Manager Contractor
Freelance Clinical Project Manager Contractor
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Job Description
Our client CRO is looking for a Freelance Clinical Project Manager with early phase Oncology experience on a 1 FTE for a duration of 612 months (with possibility to extend). This is a fully homebased role with the candidate ideally based in Sydney Melbourne or Brisbane.
What Youll Do:
Manage all aspects of assigned projects including planning execution evaluation prioritization reporting and ensuring timely delivery.
Serve as the main contact for sponsors and internal teams on assigned projects.
Assist Business Development in preparing project plans cost estimates RFP responses and participating in client presentations.
Provide accurate input for contracts including confidentiality agreements letters of intent indemnity forms service contracts and work orders.
Guide the project team on deliverables as outlined in contracts and project documents.
Oversee the preparation of essential study documents including protocols amendments CRFs consent forms and other required clinical trial documentation.
Manage daily study operations including vendor management and activity coordination.
Ensure timely review and approval of monitoring reports and address any followup actions.
Develop and implement patient recruitment and retention strategies for assigned studies.
Prepare and manage study budgets handle purchasing and transactions prepare client invoices and track payments. Work with the Head of Global Clinical Operations on team utilization rates.
Set up and maintain project requirements in the Clinical Trial Management System and other relevant systems.
Engage in additional activities like writing SOPs participating in team meetings and contributing innovative ideas.
What Youll Have:
A degree in Life Sciences (e.g. Biology Chemistry Pharmaceuticals).
Strong experience as a Project Manager in clinical research within the Pharmaceutical Biotechnology industry and ideally CROs.
Demonstrated experience in vendor management.
Deep knowledge of ICHGCP requirements across different jurisdictions.
Understanding of clinical trial budgets contracts and client billing.
Experience in Oncology is mandatory.
Ability to work in an international environment with internal and external teams
Skills in managing challenging people/clients.
Strategic and tactical thinking about drug/device development and its impact on clients.
Ability to handle and oversee multiple tasks and projects simultaneously with strong prioritization skills.
Ability to build strong relationships with management clients and crossfunctional teams fostering collaboration and longterm partnerships.
Experience leading matrix or projectbased teams.
Application closes 15 September 2024. Only shortlisted candidates may be notified.
Employment Type
Full Time
