Clinical Site Manager
- 応募
- 求人を送信
- 求人を保存
Bullet points
Industry Leading Biopharma Company in the Development of Anti-Cancer Therapies
Contribute to Global Clinical Study Programs across JAPAC Region
企業情報
- Industry leading global biopharmaceutical company in the field of oncology, immunology, infectious diseases and cardiovascular with additional therapeutic expertise in other crucial disease areas
職務内容
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Overview and conduct clinical trials in accordance with the regulatory requirements related to clinical trials, such as ICH / GCP, guidelines, standard operating procedures (SOP), site monitoring plan (SMP), trial protocol, and other applicable regulatory requirements and guidance
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Collaborate with study team members to manage the progress of their work in conducting clinical trials
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Predict, identify, and resolve overall problems / issues at the trial institution level
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Develop ways to make the most of your budget and resources and work with senior site managers, site managers and line managers to help you reach your goals
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Work closely with the rest of the company and manage the progress of exams in order to work on changes in business processes or roles that increase the value of the work, and achieve the goals of role projects that promote work efficiency
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Collect and select information on medical institutions / investigators who can conduct clinical trials appropriately
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Work with senior site managers and site monitors to develop a case registration strategy along a timeline and manage progress
理想の人材
- Demonstrates thorough understanding and knowledge of all steps in the clinical research process
- Knowledge of GCP, ICH as well as local regulations
- Experience in leading or participating as an active member of cross functional teams, task forces, or local and global initiatives Site Manager
- Extensive industry related experience as study team leader with ability to manage basic discussions in English within the responsible job-related topics, can join discussions in a global meeting, either in face-to-face or through phone
条件・待遇
- Flexible working arrangements
- Opportunity for overseas secondment
- Internal transfer opportunities within different functions
- Contribute to development of life-changing medicines across a number of core therapeutic areas