Clinical Scientist - Level Dependent Upon trabajo Madrid,Andalucia oferta de empleo Servicios Médicos España.,CTI Clinical Trial and

Puesto: Clinical Scientist - Level Dependent Upon Experience

Perform medical monitoring activities under the oversight of a medical director. Medical monitoring activities include but not limited to review of the protocol and investigator’s brochure, review of medical budgets, preparing the medical monitoring plan, training project teams on the protocol, informing site identification and feasibility activities, supporting sites with clinical questions, participating in medical meetings, participating in medical and safety data review and analysis, and preparing and presenting data to internal and external stakeholders.
Provide guidance to clinical teams on the medical and scientific aspects of assigned projects.
Analyze and synthesize clinical information, participate in clinical problem-solving and clinical decision-making in the setting of clinical trials and studies.
Lead and participate in medical data and safety reviews, including identifying critical safety trends and following up with sites/investigators to obtain additional information and to assess clinical events.
Ensure patient safety and clinical trial integrity.
Lead project-specific and department-wide organizational activities to optimize the efficiency and quality of medical services in Medical Affairs

What You'll Do:

Perform medical monitoring activities under the oversight of a medical director. Medical monitoring activities include but not limited to review of the protocol and investigator’s brochure, review of medical budgets, preparing the medical monitoring plan, training project teams on the protocol, informing site identification and feasibility activities, supporting sites with clinical questions, participating in medical meetings, participating in medical and safety data review and analysis, and preparing and presenting data to internal and external stakeholders.
Provide guidance to clinical teams on the medical and scientific aspects of assigned projects.
Analyze and synthesize clinical information, participate in clinical problem-solving and clinical decision-making in the setting of clinical trials and studies.
Lead and participate in medical data and safety reviews, including identifying critical safety trends and following up with sites/investigators to obtain additional information and to assess clinical events.
Ensure patient safety and clinical trial integrity.
Lead project-specific and department-wide organizational activities to optimize the efficiency and quality of medical services in Medical Affairs

What You'll Bring:

Ability to make clinical decisions under the oversight of an MD, ability to work in collaboration with medical professionals.
Ability to apply clinical/patient care experience to the research setting in the context of clinical trials.
Ability to integrate scientific medical data with superior written and oral communication skills.
Ability to communicate effectively (both verbally and in writing); ability to assimilate complex medical and/or research information; ability to analyze and interpret scientific data.
Working knowledge of scientific and research principles and techniques of data analysis, interpretation, and clinical relevance
Working knowledge electronic data capture systems and data visualization tools
Working knowledge of Code of Federal regulations, ICH Guidelines, Good Clinical Practice, and applicable US regulatory guidance
Ability to work effectively both independently and in a team setting to develop high quality, scientifically rigorous materials, and presentations.
Working knowledge of Microsoft Office Suite including Word, PowerPoint, Excel, One Note, as well as Access, Adobe, SharePoint, and others. Ability to become proficient in new software applications.
Working knowledge of basic business-related financial and business development…