Pharmacovigilance Associate - Remote with Onsite Onboarding

Spectraforce Technologies, Inc.; Cary (NC); Remote; USD 39,000 - 50,000; Part time

Job summary

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.

Qualifications

• 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.

Responsibilities

• 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.

Skills

Written communication

Verbal communication

Time management

Organizational skills

Detail oriented

Multi-tasking

Excel

Computer skills

Interpersonal skills

Education

Bachelor's degree or commensurate experience

Tools

Excel

Job description

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.