Fladger Associates is looking for Quality Control/Data Specialist in St Joseph, MO. This local job opportunity with ID 3662780391 is live since 2026-05-04 14:28:34.

St Joseph, MO

Contract Duration: 6-24 months

Rate: Negotiable

Salary: NA $1.00

Responsibilities:

• Excellent employment opportunity for a Quality Control/Data Specialist in the St Joseph, MO area.
• Will enter assist with data entry, reporting, and monitoring tasks to support the timely registration of new pharmaceutical products and the maintenance of existing product licenses.
• Work may include auditing of raw data, entering data into pharmacovigilance forms, auditing spreadsheets, creating tables for reports, and auditing reports.
• Direct interaction with veterinary clinics to gather information or perform QC tasks may be required.
• The individual will work with other members of the monitoring team to ensure that studies are reported in compliance with regulatory requirements and to the highest standard.
• Screen veterinary patient data for health abnormalities and enter relevant data into a PV database Cross reference data from difference sources
• Create and review report tables for data accuracy and completeness
• Perform quality audits of spreadsheets and reports
• Assist with organization and processing of raw data
• Fill in for other members of the monitoring team as needed

Experience:

• Bachelor's Degree and 3-5 years of relevant experience
• Proficient in Microsoft Suite products (i.e. MS Excel, MS Word, MS Powerpoint, MS Teams)
• Familiarity with medical terminology and veterinary medications preferred Strong written communication skills
• Excellent oral and interpersonal skills with demonstrated ability to work as part of a team
• The job will require occasional to frequent on-site work in Athens, GA
• Strong organizational skills and detail-oriented desired
• Ability to audit own work and that of others for errors
• Ability to prioritize multiple tasks and work independently
• Knowledge of Good Clinical Practices and Good Documentation Practices
• Knowledge of Regulatory Affairs and Pharmacovigilance systems a plus