Clinical Trial Leader
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Proclinical has a brilliant opportunity for a Clinical Trial Leader to be based in Brussels on a contract basis. This job will be with one of the largest workforce management solutions companies in the world who specialise in multiple scientific and engineering sectors. This individual will be responsible for clinical trial management within the Clinical R&D Operations CoE, as well as fostering strong, productive relationships with colleagues across the organisation. Serves as the liaison with the Clinical R&D Franchise for projects under his/her responsibility.
Job Responsibilities:
- Serve as a Clinical Trials Manager within the Clinical R&D Operations CoE group to execute company sponsored clinical trials for the Medical Device Franchises
- Manage all operational activities of assigned clinical trials/programs within the Clinical R&D Operations group
- Serves as a member of the clinical trial/study/program core team and may serve as the back-up liaison to the Clinical R&D Franchise and Clinical R&D BSDM for projects/trials/programs under his/her responsibility
- Independently solves problems arising during clinical trial execution.
- Manage all operational activities of assigned clinical studies within the Clinical R&D Operations group
- Provide internal communication of important clinical data and events.
- Plan, track and manage assigned projects budgets to ensure adherence to business plans
- Support the implementation of new clinical systems/processes, and provide support for publications, as needed.
- Ensure personal and company compliance with all Federal, State, local and company regulations, policies and procedures for Health, Safety, and Environmental compliance
- Provide primary leadership within a clinical trial, ensuring that each team member has a well-defined set of activities and objectives specific to their role and responsibilities within the context of their business focus.
- Manage and mentor Clinical Trial Leaders/Sr. Clinical Trial Leaders/Staff Clinical Trial Leaders.
- Accountable for quality, compliance with regulations and company procedures, resource requirement, timelines and budgets for assigned clinical projects, including those assigned to direct reports.
- Exhibit proficiency and act as a Subject Matter Expert in clinical trials involving complex design issues. May provide solutions and guidance on complex situations.
- Identify and ensure strategies, resources, and accountabilities are in place to achieve rapid, cost-effective, and high-quality execution of assigned clinical studies/programs, including those assigned to direct reports.
Skills and Requirements:
- Requires knowledge of Good Clinical Practices
- Knowledge and application of regulations and standards applied in clinical areas/regions is required.
- Strong project management skills with ability to handle multiple projects
- Strong people management skills
- Written and oral communication skills
- Know and follow all laws and policies that apply to one's job, and maintain the highest levels of professionalism, ethics and compliance at all times.
- Masters or equivalent required. Preferably in Life Science, Nursing or Biological Science.
- 8 -10 years of relevant experience or equivalent required.
- Minimum of 2 years people management.
- Significant previous experience in clinical project leadership across multiple studies/programs required.
- Experience with budget planning, tracking and control required.
- Need to be on site several days a week
To Apply:
Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.
In case you have difficulty in applying or if you have any questions, please call Sasha Brasero on +44 203 078 9556 or upload your CV on our website - www.Proclinical.com.
A full job description is available on request.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
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