Pharmacovigilance Associate

Spectraforce Technologies, Inc.; Cary (NC); Teletrabalho; USD 39 000 - 50 000; Tempo parcial

Resumo da oferta

Spectraforce Technologies, Inc. is seeking a Pharmacovigilance Associate located near Cary, NC. The role involves creating and submitting adverse event reports and product complaints from data in our patient management system.

Oncology experience and a clinical background are a plus. The assignment runs for five months with remote work after an initial onboarding period on site, and requires strong attention to detail and effective communication with clinicians.

Qualificações

• Bachelor's degree or commensurate experience preferred.
• Experience in pharmacy or pharmacovigilance preferred.
• Oncology experience a plus.
• Pharmacy technician or clinical background preferred.
• Prior pharmacovigilance experience preferred.
• Strong written and verbal communication skills.
• Excellent organizational and time management skills.
• Proficient with computers and Excel.

Responsabilidades

• Create and submit adverse event and product complaint reports from data in the patient management system.
• Perform quality checks on information, spelling, drug, manufacturer and grammar.
• Communicate with clinicians regarding questions about adverse event reporting.
• Identify missing adverse events and product complaints and report to clinicians.
• Ensure missing reports are submitted and accounted for.
• Submit weekly or monthly reconciliation reports to biopharma clients as per contracts.
• Assist clinical auditor in identifying trends or issues in reporting.
• Perform other duties as assigned.

Conhecimentos

Written communication

Verbal communication

Time management

Organizational skills

Detail oriented

Multi-tasking

Excel

Computer skills

Interpersonal skills

Formação académica

Bachelor's degree or commensurate experience

Ferramentas

Excel

Descrição da oferta de emprego

Position Title: Pharmacovigilance Associate

Work Location: Candidate must be local to Cary, NC (within a 60-mile radius)

Assignment Duration: 5 Months

Work Schedule: 9:00am-6:00pm eastern or 10:00am-7:00pm eastern

Work Arrangement: Remote: 1 week of onsite onboarding at Cary, NC, then 1 week of one-on-one training with Lead onsite. Then fully remote afterwards.

Position Summary: Creating and submitting adverse event and product complaint reports from data documented within our patient management system.

Key Responsibilities:

• Creating and submitting adverse event and product complaint reports from data documented within our patient management system.
• Conduct quality check (QC) of information, spelling, drug, manufacturer and grammar included in the note.
• Communicating with clinicians regarding questions or concerns with the content or quality of adverse event reporting.
• Identify through the daily QC process and report any missing adverse events (AEs) and product complaints (PCs) to clinicians
• Ensure that any identified missing reports have been submitted and accounted for
• Maintain and submit weekly or monthly reconciliation reports to biopharma clients in accordance with client contracts
• Assist clinical auditor in identifying trends or issues in adverse event reporting
• Perform other duties as assigned

Qualification & Experience:

• Bachelor's degree or commensurate experience preferred
• Prior experience working in a Pharmacy setting preferred
• Oncology experience a plus
• Pharmacy technician or other clinical background preferred
• Prior experience with pharmacovigilance strongly preferred
• Excellent written and verbal communication skills
• Excellent organizational and time management skills
• Competent in moderate to advanced computer skills
• Competent in excel spreadsheets
• Multi-task oriented
• Ability to effectively work with people
• Conscientious with excellent attention to detail
• Flexible and adaptable
• Essential to be able to type rapidly and accurately both numerical and text data.