Planet Pharma are working with a leading, global CRO which are seeking several Senior Clinical Trial Managers on a permanent basis.
Why join them?
My client is a diverse, growing, global company where people excel. Their employees work in a fast-paced, creative environment where learning is a constant. You will be exposed to a world of experiences with fantastic career progression.
Working on complex therapeutic areas – Oncology, Gene and Cell Therapy, Cardiology, Neurology.
The Profile:
Provide leadership and direction to project team members.
Identify, organize and deliver (where appropriate) study specific training in collaboration with Project Leader and Project Specialists.
Evaluate and identify resourcing needs and continuously monitor the use of resources over life cycle of large/complex project and/or program.
Provide productivity targets to project team members.
Provide performance feedback on team members as appropriate.
Address identified and escalated site issues and drive to closure.
Early recognize areas of potential problems and provide input to contingency plans.
Monitor study timelines, patient recruitment, retention and data cleaning to ensure successful outcome of the project and/or program.
Proactively plan and manage large/complex or multiple projects within a program (ability to prioritize multiple timelines and deliverables simultaneously).
Oversee maintenance and quality check of Central Files.
Maintain and assure quality of work generated and escalate and follow up as appropriate.
Ensure appropriate handover between project team members with support from Clinical Operations Managers.
Implement and instigate process improvements within the project.
Provide input to the Revenue Recognition forecast.
Identify changes in scope and liaise with Project Leader.
May be required to conduct site visits as per client or project demands.
Participate in client, investigator and team meetings.
Prepare, participate in and follow up on audits / inspections.
Participate in all required applicable trainings.
The Ideal Candidate Will Have:
Must hold a life science or medical-related degree or equivalent qualification.
Previous cross-functional clinical trial management experience in a CRO, Biotech or Pharmaceutical Company at an international/global level.
Experience in clinical trial planning and conduct.
Thorough knowledge of ICH-GCP and applicable local/regional regulations.
Experience of leading global Phase II-III clinical trials, with experience in oncology or adaptive/innovative trial design preferred but not mandatory.
To apply:
For more information on this position or any similar opportunities, please contact Michael Popoola on 0204 542 4275 or email your CV and we can arrange a time for a confidential discussion about your career step.
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