.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
