Quality Control/Data Specialist -- US2710 : Clin Pharma STJ at OQSIE
St. Joseph, MO
About the Job
Description: The Quality Control/Data Specialist 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.
Major Responsibilities:
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
Minimum Qualifications:
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
Desired Skills:
Strong organizational skills and detail oriented
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
Major Responsibilities:
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
Minimum Qualifications:
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
Desired Skills:
Strong organizational skills and detail oriented
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