Clinical Trial Coordinator

Clinical Trial Coordinator

Clinical Trial Coordinator

Thermo Fisher Scientific

1 hora atrás

Nenhuma candidatura

Sobre

  • 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.