Data Analyst V

Spectraforce Technologies, Inc.; Duluth (GA); On-site; USD 75,000 - 110,000; Full time

Job summary

Spectraforce Technologies, Inc. is seeking a Data Analyst V in Duluth, GA to perform pharmacovigilance signal detection and analysis, generating monthly and quarterly trending reports and supporting regulatory submissions for internal stakeholders.

The role requires fluent English, knowledge of pharmacovigilance, epidemiology or statistics, experience in highly regulated environments, and strong Microsoft Office proficiency; you will contribute to PV surveillance and risk management activities.

Qualifications

• Fluent in written and spoken English.
• Knowledge of pharmacovigilance, epidemiology, statistics or related field.
• Experience working in a highly regulated environment.
• High level of computer literacy and fluent in Microsoft Office platforms.

Responsibilities

• Performs Pharmacovigilance signal detection and analysis including generation of monthly and quarterly trending reports.
• Performs data analysis and report generation for ad hoc requests for PV information to support regulatory authority requests and stakeholder support (marketing, quality, external customers, etc.).
• Contributes to other PV product surveillance and risk management activities as needed.

Skills

English fluency

Pharmacovigilance

Epidemiology

Statistics

Regulated environment

MS Office

Tools

Microsoft Office

Job description

Position Title: Data Analyst V

Work Location: Duluth, GA 30096

Assignment Duration: 12 Months

Work Arrangement: Onsite at one of our organization's sites (Athens GA, Johns Creek GA, Gainesville GA, St Joseph MO, Ames IA)

Position Summary: Performs Pharmacovigilance signal detection and analysis including generation of monthly and quarterly trending reports.

Key Responsibilities:

• Performs Pharmacovigilance signal detection and analysis including generation of monthly and quarterly trending reports.
• Performs data analysis and report generation for ad hoc requests for PV information to support regulatory authority requests and stakeholder support (marketing, quality, external customers, etc.).
• Contributes to other PV product surveillance and risk management activities as needed.

Qualification & Experience:

• Fluent in written and spoken English
• Knowledge of pharmacovigilance, epidemiology, statistics or related field.
• Experience working in a highly regulated environment
• High level of computer literacy and fluent in Microsoft Office platforms