Co-op, Pharmacovigilance Scientist

Role Summary

Co-op, Pharmacovigilance Scientist will be an integral member of the PV/Safety team focused on patient safety, compliance, and continuous improvement in a fast-paced biotech/pharma environment. You will gain hands-on experience in PV/Safety science and contribute to literature review, safety data analysis, and aggregate safety reports to evaluate safety data and understand evolving product safety profiles. This role will help you learn the principles of safety surveillance and compliance with global PV regulations and guidance.

Responsibilities

• Actively participate in team meetings and assist with meeting minutes
• Support PV projects, resolve pending action items and track their status
• Support the clinical scientific literature review and monitoring
• Support the review and analysis of safety data arised from various sources
• Support the authoring and revision of scientific documents including aggregate safety reports
• Contribute to process improvement activities within the PV/Safety team.

Qualifications

• Demonstrated experience in analysis and interpretation of clinical and/or scientific data
• Advanced skills in Microsoft Office applications including Excel, SharePoint, Power Point, Word, MS Teams
• Strong analytical skills
• Team player who desires to collaborate with pharmacovigilance/safety and cross functional team members
• Excellent written and verbal communication
• Willingness to learn, be mentored, and improve

Education

• Third year or higher into Advanced Degree programs (Ph.D. in life science (e.g. Biology, Pharmacology, Toxicology, Epidemiology), or NP, or PharmD) required
• Prior experience of scientific publications (Abstracts and or journal articles) preferred

Additional Requirements

• Legal authorization to work in the U.S.
• At least 18 years of age prior to the scheduled start date.
• Currently enrolled in an accredited community college, college, university or skills program/apprenticeship.