Clinical Study Scientist I – Lab Processing

Abbott; Madison (AL); On-site; USD 28,000 - 56,000; Full time

Job summary

Abbott in Madison, WI, is seeking a Clinical Study Scientist I to support clinical trials in the Cancer Diagnostics division. The role involves processing samples, performing analytical testing, and documenting QA activities.

You will operate instruments, manage specimen handling, and collaborate with the Clinical Study Team to ensure timely results and data integrity. This position requires a bachelor’s in life sciences, 1+ year experience with human samples, and US work authorization;

Qualifications

• Bachelor’s degree in Biology, Chemistry, Biochemistry, Microbiology, Molecular Biology, Clinical Laboratory Sciences, or a similar life sciences degree.
• 1+ years of experience with human samples after receiving a Bachelor’s degree.
• Demonstrated knowledge of HIPAA, GLP, and GDP.
• Ability to use Microsoft Office Programs.
• Authorization to work in the United States without sponsorship.

Responsibilities

• Process and accession clinical trial samples and ensure validity.
• Operate and maintain laboratory instruments and automation.
• Document QA/QC activities and equipment maintenance.
• Follow schedule and report issues to Lab Leadership.
• Maintain safety and data security, and uphold quality systems.
• Travel up to 10% of time.

Skills

HIPAA knowledge

GDP knowledge

Microsoft Office

US work authorization

Education

Bachelor’s degree in Biology, Chemistry, Biochemistry, Microbiology, Molecular Biology, Clinical Laboratory Sciences, or a similar life sciences degree

Job description

Abbott in Madison, WI, is seeking a Clinical Study Scientist I to support clinical trials in the Cancer Diagnostics division. The role involves processing samples, performing analytical testing, and documenting QA activities.

You will operate instruments, manage specimen handling, and collaborate with the Clinical Study Team to ensure timely results and data integrity. This position requires a bachelor’s in life sciences, 1+ year experience with human samples, and US work authorization;