Pharmacovigilance Data Specialist: Drug Safety & Reporting

SGS Consulting; New York (NY); On-site; USD 70,000 - 90,000; Full time

Job summary

SGS Consulting seeks a pharmacovigilance specialist to support safety reporting duties, including case processing, adverse event reviews, and regulatory submissions, within a collaborative team. The role requires a health care professional background and a bachelor’s in science; English fluency is essential.

Experience in data management and medical writing is advantageous, with strong computer literacy and database skills valued.

Qualifications

• Experience in pharmacovigilance and/or data management
• Experience and skill in medical writing is an advantage
• Demonstrated computer literacy; relational databases experience

Responsibilities

• Review, preparation, and completion of reports of adverse drug experiences
• Determine local submission of safety reports
• Carry out case processing activities and document case information
• Liaise with partners locally and with stakeholders regarding safety data collection and reconciliation

Skills

Pharmacovigilance

Data management

Medical writing

Computer literacy

Relational databases

Education

Bachelor’s degree in science

Health Care Professional or equivalent

Job description

SGS Consulting seeks a pharmacovigilance specialist to support safety reporting duties, including case processing, adverse event reviews, and regulatory submissions, within a collaborative team. The role requires a health care professional background and a bachelor’s in science; English fluency is essential.

Experience in data management and medical writing is advantageous, with strong computer literacy and database skills valued.