Remote, São Paulo, Brazil
18 hours ago
Clinical Trial Coordinator

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Provides administrative and technical support to the Project Team. Supports audit readiness by ensuring files are reviewed according to the schedule 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 CRG personnel. May utilize local knowledge, organization systems, external site lists and sponsor directives to develop and review site lists that are suitable for the strategic needs of feasibility activities and to provide local input into the site tiering process. May act as a buddy during onboarding phase and provide training to new staff as needed.

Qualifications:Education and Experience: High / Secondary school diploma or equivalent and relevant formal academic / vocational
qualification. 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 directly
related 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 to 
detail, with proven ability to handle multiple tasks efficiently and effectively 
Demonstrated ability to effectively analyze project-specific 
data/systems to ensure accuracy and efficiency 
Strong customer focus 
Flexibility to reprioritize workload to meet changing project 
timelines 
Demonstrated ability to attain and maintain a good working knowledge of applicable Country Regulations, ICH Good Clinical 
Practices, 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 successfully 
complete the organizations clinical training program 
Self-motivated, positive attitude and good interpersonal skills Effective oral and 
written 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 appropriately.

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