Technician, R&D IV, Project Coordinator
Posted on Oct 5, 2024 by AbbVie
North Chicago, IL
Admin & Secretarial
Immediate Start
Annual Salary
Full-Time
Job Description
Purpose: Proficiently manage the report coordination of Toxicology and Pathology reports within Nonclinical. Working cross-functionally with Study Directors, Pathologists, QA, and Report Publishing to develop and execute reports.
Responsibilities:
Oversee communication with Study Directors, Tox Associates, Pathologists, and Support Pathology Staff to ensure the accurate capture of information and components within the reports.
Coordinate and manage multiple reports. Proactively anticipate obstacles and collaborate with the team to formulate solutions.
Conduct thorough quality assessments of published output, ensuring alignment with regulatory standards and health authority guidance. Verify content, including bookmarks, hyperlinks, and tables of content.
Contribute to the development of optimal business processes and standards within the department, ensuring robust stakeholder support to achieve high quality reports.
Position accountability/scope:
Regularly engage with the manager to discuss project priorities, timelines, progress and identified challenges.
Manage projects with oversight as necessary.
Provide training and cross-train with other team members to offer additional support as required.
Purpose: Proficiently manage the report coordination of Toxicology and Pathology reports within Nonclinical. Working cross-functionally with Study Directors, Pathologists, QA, and Report Publishing to develop and execute reports.
Responsibilities:
Oversee communication with Study Directors, Tox Associates, Pathologists, and Support Pathology Staff to ensure the accurate capture of information and components within the reports.
Coordinate and manage multiple reports. Proactively anticipate obstacles and collaborate with the team to formulate solutions.
Conduct thorough quality assessments of published output, ensuring alignment with regulatory standards and health authority guidance. Verify content, including bookmarks, hyperlinks, and tables of content.
Contribute to the development of optimal business processes and standards within the department, ensuring robust stakeholder support to achieve high quality reports.
Position accountability/scope:
Regularly engage with the manager to discuss project priorities, timelines, progress and identified challenges.
Manage projects with oversight as necessary.
Provide training and cross-train with other team members to offer additional support as required.
Reference: 203338671
https://jobs.careeraddict.com/post/95818604
Technician, R&D IV, Project Coordinator
Posted on Oct 5, 2024 by AbbVie
North Chicago, IL
Admin & Secretarial
Immediate Start
Annual Salary
Full-Time
Job Description
Purpose: Proficiently manage the report coordination of Toxicology and Pathology reports within Nonclinical. Working cross-functionally with Study Directors, Pathologists, QA, and Report Publishing to develop and execute reports.
Responsibilities:
Oversee communication with Study Directors, Tox Associates, Pathologists, and Support Pathology Staff to ensure the accurate capture of information and components within the reports.
Coordinate and manage multiple reports. Proactively anticipate obstacles and collaborate with the team to formulate solutions.
Conduct thorough quality assessments of published output, ensuring alignment with regulatory standards and health authority guidance. Verify content, including bookmarks, hyperlinks, and tables of content.
Contribute to the development of optimal business processes and standards within the department, ensuring robust stakeholder support to achieve high quality reports.
Position accountability/scope:
Regularly engage with the manager to discuss project priorities, timelines, progress and identified challenges.
Manage projects with oversight as necessary.
Provide training and cross-train with other team members to offer additional support as required.
Purpose: Proficiently manage the report coordination of Toxicology and Pathology reports within Nonclinical. Working cross-functionally with Study Directors, Pathologists, QA, and Report Publishing to develop and execute reports.
Responsibilities:
Oversee communication with Study Directors, Tox Associates, Pathologists, and Support Pathology Staff to ensure the accurate capture of information and components within the reports.
Coordinate and manage multiple reports. Proactively anticipate obstacles and collaborate with the team to formulate solutions.
Conduct thorough quality assessments of published output, ensuring alignment with regulatory standards and health authority guidance. Verify content, including bookmarks, hyperlinks, and tables of content.
Contribute to the development of optimal business processes and standards within the department, ensuring robust stakeholder support to achieve high quality reports.
Position accountability/scope:
Regularly engage with the manager to discuss project priorities, timelines, progress and identified challenges.
Manage projects with oversight as necessary.
Provide training and cross-train with other team members to offer additional support as required.
Reference: 203338671
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