Protocol Manager (Oncology)
- Permanent
- Clinical Operations, Project Management
This vacancy has now expired. Please see similar roles below...
Hobson Prior are currently looking for a Senior Clinical Research Associate to join a Global CRO at their offices in Belgium on a permanent basis. This role will support overall project management of clinical studies by helping control the scope, schedule and cost of assigned projects, which may range from single service studies to full scope or multiple protocol projects.
Job Responsibilities:
- Accountable to create and maintain the Trial Master File Management Plan.
- Routinely reviews the TMF to ensure quality, completeness and inspection readiness.
- Organises and monitors the activities associated with study deliverables across all applicable internal functional departments and vendors.
- Assists with activities associated with interim analyses, database snapshots and locks, final CSR and study closure.
- Assists with identification of and contracting with approved vendors, as necessary.
- Develops contingency planning and risk mitigation strategies to ensure meeting or exceeding study milestones.
- Creation and maintenance of metric reports, inclusive of data collection from multiple sources, for delivery to client or senior management.
- Assists with overall financial performance of the study by interacting with internal functional departments or vendors to obtain required metrics for financial reporting.
- Partakes in representing the company to the client, ensuring satisfaction levels are met and statuses of deliverables are communicated effectively.
- Facilitates team training in accordance with protocol and/or project requirements, including therapeutic, protocol specific, and process training.
- Develops knowledge of current therapeutic environment.
Key Skills:
- Strong organizational skills.
- Strong ability to manage time and work independently.
- Excellent communication, presentation, interpersonal skills, both written and spoken, with an ability to inform, influence, convince and persuade.
- Flexibility and ability to handle multiple tasks to meet deadlines while delivering high quality work in a dynamic environment.
- High level of competency in English language.
- Proficiency with MS Office Applications.
Requirements:
- Bachelor's Degree (or equivalent) level of qualification in Life Sciences, Medicine, Pharmacy, Nursing or related field equivalent preferred
- Prior experience in a contract research organization (CRO), pharmaceutical, or biotechnology company preferred. CRO and relevant therapeutic experience preferred
- Strong knowledge of Good Clinical Practice/ICH guidelines and other applicable regulatory requirements
- Ability to travel as necessary (up to 25%)
Apply now:
If you are interested in learning more or applying to this exciting opportunity, please complete the form below and attach a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist, please request a call back at the top of this page.
Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.
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