Clinical Trial Coordinator

Titulo da Vaga: Clinical Trial Coordinator

Localização: São Paulo – SP

Descrição da Vaga: Work Schedule Standard (Mon-Fri)Environmental Conditions OfficeJob DescriptionProvides administrative and technical support to the Project Team. Supports audit readiness by ensuring files are reviewed according to theschedule detailed in the organization’s SOP and department guidance document. Provides administrative support for site activation activities.Aids the development of the critical path for site activation within assigned projects in support of rapid site activations. Represents CRGpersonnel. May utilize local knowledge, organization systems, external site lists and sponsor directives to develop and review site lists thatare suitable for the strategic needs of feasibility activities and to provide local input into the site tiering process. May act as a buddy duringonboarding phase and provide training to new staff as needed.Qualifications:Education and Experience: High / Secondary school diploma or equivalent and relevant formal academic / vocationalqualification. Bachelor’s degree preferred. Previous experience that provides the knowledge, skills, and abilities to perform the job(comparable to 0 to 1 year). In some cases an equivalency, consisting of a combination of appropriate education, training and/or directlyrelated experience, will be considered sufficient for an individual to meet the requirements of the role.Knowledge, Skills and Abilities: 􀀀Ability to work in a team or independently as required 􀀀Good organizational skills and strong attention todetail, with proven ability to handle multiple tasks efficiently and effectively 􀀀Demonstrated ability to effectively analyze project-specificdata/systems to ensure accuracy and efficiency 􀀀Strong customer focus 􀀀Flexibility to reprioritize workload to meet changing projecttimelines 􀀀Demonstrated ability to attain and maintain a good working knowledge of applicable Country Regulations, ICH Good ClinicalPractices, and organization/Client SOPs and WPDs for all non-clinical/clinical aspects of project implementation, execution and closeout􀀀Good English language and grammar skills and proficient local language skills as needed 􀀀Good computer skills, proficient in MS Office(Word, Excel, and PowerPoint) and ability to obtain knowledge and master all clinical trial database systems 􀀀Ability to successfullycomplete the organizations clinical training program 􀀀Self-motivated, positive attitude and good interpersonal skills 􀀀Effective oral andwritten communication skills 􀀀Good interpersonal skills 􀀀Essential judgment and decision-making skills 􀀀Capable of accurately following project work instructions 􀀀Good negotiation skills 􀀀Independent thinker 􀀀Ability to manage risk and perform risk escalation appropriatelyhas context menu

Nome da Empresa: Thermo Fisher Scientific

Salário:

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