Clinical Trials Operations Associate

Regulatory Jobs; Madison (WI); On-site; USD 51,000 - 101,000; Full time

Job summary

Abbott in Madison, Wisconsin is seeking a Clinical Trial Assistant/Coordinator to support the execution of clinical trials. You will coordinate with the Clinical Affairs team and external sites, manage study trackers, and assist with study documents and data management tools.

The role requires a Bachelor’s or related degree and knowledge of GCP/ICH guidelines, with duties spanning from study start-up to close-out and cross-functional collaboration.

Qualifications

• General knowledge of clinical research principles and requirements, including GCP and ICH guidelines.
• Proficient in basic software applications including Word, Excel, and Outlook.
• Ability to perform essential duties with or without accommodation.

Responsibilities

• Assist in execution of clinical trials with quality administrative and project management support.
• Coordinate with Clinical Affairs team and internal/external stakeholders to execute study plans.
• Create and maintain study trackers and conduct data management related tasks.

Education

Bachelor’s degree in the life sciences or related field; or Associates degree in the life sciences or related field and 2 years of relevant experience in lieu of Bachelor’s degree

Tools

Microsoft Office

Job description

Abbott in Madison, Wisconsin is seeking a Clinical Trial Assistant/Coordinator to support the execution of clinical trials. You will coordinate with the Clinical Affairs team and external sites, manage study trackers, and assist with study documents and data management tools.

The role requires a Bachelor’s or related degree and knowledge of GCP/ICH guidelines, with duties spanning from study start-up to close-out and cross-functional collaboration.