Bilingual Pharmacovigilance Associate — Remote

BioScript Solutions; Town of Woodstock; Vor Ort; CAD 60.000 - 75.000; Vollzeit

Benefits dieser Stelle

Flexible remote work

Growth opportunities

Vibrant culture

Competitive compensation & benefits

Zusammenfassung

BioScript Solutions seeks a meticulous Pharmacovigilance Associate to join our Patient Support Programs and help manage adverse event reporting with high compliance and accuracy. The role supports CAPA activities and safety case processing while coordinating with cross-functional teams.

Remote, full-time on a 6-month contract; bilingual English/French required; CBC alignment and data integrity are emphasized.

Qualifikationen

• BSc and/or BA related to Health Science.
• 1-3 years of PV/Medical Information/Adverse Event Reporting/Safety Case Processing experience and/or Regulatory or QA is an asset.
• Good understanding of safety regulations.
• Experience in medical and/or pharmaceutical field(s), including exposure to medical terminology and/or scientific writing is an asset.
• Exceptional organizational skills and strong attention to detail.
• Proven analytical and proven solving skills.
• Preference for an individual with CAPA investigation experience.
• Versed in Change Control Management is an asset.
• Proficient in conducting Program Compliance.
• Above average verbal and written communication skills.
• Demonstrated prioritization skills and ability to multi-task to meet tight deadlines.
• Bilingual, English/French is required.
• Comfortable working with computers and the Microsoft Office suite.

Aufgaben

• Manage the collection, processing, and reporting of adverse events (AEs) and reconciliation reports.
• Accountable for recognizing, triaging, and reporting as per the program or manufacturer requirements.
• Maintain high compliance standards regarding reporting timelines, quality of reporting, and responding to inquiries from stakeholders.
• Help conduct Pharmacovigilance compliance activities.
• Assisting in the initiation of investigations for late AE reports.
• Shift Rotation–8:00a.m.-4:00p.m. EST, 9:00a.m.-5:00p.m. EST, 10:00a.m.-6:00p.m EST. Occasional weekend work.

Kenntnisse

Pharmacovigilance experience

Analytical skills

Excellent organization

Attention to detail

Bilingual English/French

Ausbildung

BSc/BA in Health Science

Tools

Microsoft Office

Jobbeschreibung

BioScript Solutions seeks a meticulous Pharmacovigilance Associate to join our Patient Support Programs and help manage adverse event reporting with high compliance and accuracy. The role supports CAPA activities and safety case processing while coordinating with cross-functional teams.

Remote, full-time on a 6-month contract; bilingual English/French required; CBC alignment and data integrity are emphasized.