Profile:
Clinical Trial Leader
A clinical trial leader is required to conduct and be accountable for the planning and management of the clinical program from a day-to-day operational perspective to achieve strategic and operational objectives. Be responsible for the on-boarding and development of Clinical Trial Heads (CTHs) and Clinical Managers (CMs) and act as operational manager of assigned Program Operations Managers (POMs).
Responsibilities:
· To account for the development and the accuracy of the clinical program operational plan and drive execution through the organisation according to the approved overall plan
· Responsible for clinical trial resource forecast, monitoring and management
· Participate to the review and edit publications/presentations for Investigator Meetings
· Coordinate the program Safety Review Boards /Advisory Boards
· Manage the performance management process incl. annual objectives for CMs and CTHs according to program priorities, performance appraisal and individual development needs in collaboration with operational supervisors
· Contribute to the CMs and CTHs hiring plan and staffing activities
· Act as operational manager of assigned POMs to maximize contribution to GPT in collaboration with the Global Head Clinical Trial Resources
· Ensure efficient on-boarding, training and mentoring of new associates
· Identify individual CMs and CTHs training needs to foster high levels of performance; support career development through quality development plans and proactively manage performance issues
· Participate to the development and implementation to process standards and tools to achieve excellence in trial operations and management; ensure global adherence and implementation support in a manner that creates consistency, efficiency and with a high level of compliance within the department across compounds and projects
· Be an active participant on the Clinical Trial Management and Resources meeting to standardise clinical practice and share best practice
· Act as full member of the Clinical Trial Management and Resources Management Team
Qualifications & experience:
· Advanced degree or equivalent education/degree in life science/healthcare required
· Fluent English (oral and written)
· ? 8 years of pharmaceutical clinical research experience
· ? 5 years people management and development experience required
· Demonstrated leadership and accomplishment in all aspects of conducting global clinical trials and programs
· Extensive knowledge of clinical development process, GCP and clinical project management
· Organisational awareness, including significant experience working cross-functionally and in global teams
· Excellent interpersonal, problem-solving, negotiation and conflict resolution skills
· Knowledge of resource planning and management
· Basic medical/scientific knowledge of Oncology and/or Haematology
Relevant working/residency permit or Swiss/EU-Citizenship required.
For more information or to apply, please forward your CV to luke@srgclinical.com or call +44 207 562 19790
The recruiter has stated that all applicants for this job should be able to prove that they are legally entitled to work in the country where the job is based. Carlisle Staffing plc, trading as SRG is an Employment Business/Agency.
