Clinical Trial Coordinator

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Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionProvides 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 thatare 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 / 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 directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

Knowledge, Skills And AbilitiesAbility to work in a team or independently as requiredGood organizational skills and strong attention to detail, with proven ability to handle multiple tasks efficiently and effectivelyDemonstrated ability to effectively analyze project-specific data/systems to ensure accuracy and efficiencyStrong customer focusFlexibility to reprioritize workload to meet changing projecttimelinesDemonstrated 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 closeoutGood 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 systemsAbility to successfully complete the organizations clinical training programSelf-motivated, positive attitude and good interpersonal skillsEffective oral and written communication skillsGood interpersonal skillsEssential Judgment And Decision-making SkillsCapable of accurately following project work instructionsGood negotiation skillsIndependent thinkerAbility to manage risk and perform risk escalation appropriatelyThermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

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