Remote Pharmacovigilance Operations Manager

Parexel; Annapolis (MD); Remote; USD 120,000 - 150,000; Full time

Benefits offered by this job

Health, Vision & Dental Insurance

Tuition Reimbursement

Vacation/Holiday/Sick Time

Flexible Spending & Health Savings

Work/Life Balance

401(k) with Company match

Pet Insurance

Job summary

Parexel is hiring a Manager, Patient Safety Operations (Pharmacovigilance Operations Manager) for a remote role. You will lead Patient Safety staff, oversee safety processing, and ensure quality, timelines, and regulatory compliance across projects.

You’ll communicate with clients, drive process improvements, and contribute to automation initiatives. The role emphasizes team development, cross-functional collaboration, and delivering high-quality safety services essential to clinical research

Qualifications

• Strong knowledge of clinical safety services and pharmacovigilance operations.
• Experience leading teams and coaching staff in a regulated environment.
• Proven ability to interact professionally with clients and cross-functional partners.
• Familiarity with automation and AI applications in pharmacovigilance.

Responsibilities

• Manage and develop Patient Safety staff and coordinate staffing with leaders.
• Provide coaching, performance appraisals, and development plans.
• Ensure work meets SLAs, quality, and training KPIs.
• Oversee safety processes, respond to queries, and support urgent needs.
• Participate in pharmacovigilance automation tool implementation and optimization.
• Maintain knowledge of regulations, SOPs, audits, and risk mitigation.

Skills

Clinical safety

Regulatory knowledge

Pharmacovigilance operations

Line management

Client interaction

Automation/AI awareness

Education

Degree in Pharmacy, Nursing, Life Science

Tools

Pharmacovigilance automation tools

Job description

Parexel is hiring a Manager, Patient Safety Operations (Pharmacovigilance Operations Manager) for a remote role. You will lead Patient Safety staff, oversee safety processing, and ensure quality, timelines, and regulatory compliance across projects.

You’ll communicate with clients, drive process improvements, and contribute to automation initiatives. The role emphasizes team development, cross-functional collaboration, and delivering high-quality safety services essential to clinical research