Remote Pharmacovigilance Operations Manager

African American Talent

Sacramento (CA)

Remote

USD 120,000 - 170,000

Full time

2 days ago
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Benefits offered by this job

Health insurance
Tuition reimbursement
Vacation/holiday/sick time
401(k) with company match
Work/Life Balance
Flexible Spending & Health Savings

Job summary

Parexel is seeking a Manager, Patient Safety Operations to lead Pharmacovigilance operations in a remote-capacity role. You will supervise staff, ensure quality and timelines, and coordinate with clients to address questions and escalations.

You will drive process improvements, maintain regulatory knowledge, and guide cross-functional teams to deliver high-quality safety services for clinical research and patient protection.

Qualifications

  • Bachelors degree or higher in a health-related field or equivalent experience.
  • Strong knowledge of pharmacovigilance operations and clinical research methodologies.
  • Experience leading teams and coaching staff.
  • Excellent communication and client-facing skills.
  • Understanding of ICH, CIOMS, GVP, and basic pharmacovigilance requirements.

Responsibilities

  • Manage and develop Patient Safety staff, delegate work and coordinate staffing with leaders.
  • Provide coaching, development plans, and performance reviews.
  • Ensure work meets SLAs and KPIs for quality and training.
  • Oversee safety processes, respond to queries, and support urgent workloads.
  • Lead process improvements and adoption of automation and digital solutions.

Skills

Pharmacovigilance
People management
Client engagement
Project management
Regulatory knowledge

Education

Degree in Pharmacy or Life Science
Experience in Pharmacovigilance

Tools

PV software
Safety databases
Automation tools

Job description

Parexel is seeking a Manager, Patient Safety Operations to lead Pharmacovigilance operations in a remote-capacity role. You will supervise staff, ensure quality and timelines, and coordinate with clients to address questions and escalations.

You will drive process improvements, maintain regulatory knowledge, and guide cross-functional teams to deliver high-quality safety services for clinical research and patient protection.

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