Pharmacovigilance & Patient Safety Associate - Remote

Veristat; Massachusetts; Hybrid; USD 74,000 - 85,000; Full time

Benefits offered by this job

Remote working

Flexible time off

Paid holidays

Medical insurance

Tuition reimbursement

Retirement plans

Job summary

Veristat in Massachusetts is seeking a Pharmacovigilance and Patient Safety Associate to oversee processing of serious adverse events and safety matters for study participants. The role collaborates with sponsors, investigators, and internal teams to ensure accurate AE/SAE collection and reporting.

Ideal candidates hold a bachelor’s degree in science, 2–4 years in pharmacovigilance, strong knowledge of ICH GCP, excellent communication, and the ability to mentor others.

Qualifications

• Bachelor’s Degree in a science or related field required.
• 2–4 years pharmacovigilance/drug safety experience in CRO/pharma/clinical trials.
• Proficient with ICH GCP guidelines and regulatory rules; medical terminology knowledge.
• Excellent project management, written and verbal communication, organizational and interpersonal skills.
• Familiarity with safety databases; English proficiency required.
• Ability to mentor and delegate in a fast-paced environment.

Responsibilities

• Process and manage serious adverse events (SAEs) and safety matters.
• Collaborate with sponsors, investigators, and internal teams to collect and report AE/SAE information.
• Assist department head in overseeing safety group activities.
• Lead project teams and support mentoring of colleagues.

Skills

Project management

Written and verbal communication

Interpersonal skills

English proficiency

Team leadership

Education

Bachelor’s degree in science or related field

Advanced degree (PharmD/MD) preferred

Tools

Safety databases

Job description

Veristat in Massachusetts is seeking a Pharmacovigilance and Patient Safety Associate to oversee processing of serious adverse events and safety matters for study participants. The role collaborates with sponsors, investigators, and internal teams to ensure accurate AE/SAE collection and reporting.

Ideal candidates hold a bachelor’s degree in science, 2–4 years in pharmacovigilance, strong knowledge of ICH GCP, excellent communication, and the ability to mentor others.