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Job summary
A global staffing and IT consulting firm in New Jersey is seeking a Safety Specialist/Sr. Triage Associate. The role requires leading data entry for reports and necessitates at least 8 years of pharmaceutical experience, including 5 years in pharmacovigilance. An ideal candidate should have a Bachelor’s degree (Master’s preferred) in a related field, along with experience supervising teams and excellent problem-solving skills. This is a long-term position with opportunities for professional growth.
Qualifications
Bachelor’s degree in Life Science, Nursing, Regulatory Affairs, Chemistry or Pharmacy.
Minimum of 8 years pharmaceutical experience, 5+ years in pharmacovigilance.
Experience supervising and communicating with diverse teams.
Responsibilities
Lead and prioritize data entry for regulatory reporting duties.
Identify and manage clinical study cases for reports.
Train and mentor junior colleagues while ensuring compliance.
Skills
Health/life sciences mastery
AE processing expertise
Team supervision experience
Problem-solving techniques
Excellent communication skills
Education
Bachelor’s degree
Master’s degree preferred
Tools
Microsoft Suite
Job description
A global staffing and IT consulting firm in New Jersey is seeking a Safety Specialist/Sr. Triage Associate. The role requires leading data entry for reports and necessitates at least 8 years of pharmaceutical experience, including 5 years in pharmacovigilance. An ideal candidate should have a Bachelor’s degree (Master’s preferred) in a related field, along with experience supervising teams and excellent problem-solving skills. This is a long-term position with opportunities for professional growth.