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.




