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Parexel

End-to-end clinical trials and regulatory consulting

Manager, Patient Safety Operations

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeRemote in USANo salary listedRemote

About the Job

Requirements

  • A degree in Pharmacy, Nursing, Life Science, or another health-related field, or an equivalent qualification or relevant work experience.
  • People management experience.
  • Considerable experience working with clients.
  • Working knowledge of pharmacovigilance operations and clinical research methodologies.
  • Excellent clinical, regulatory, and medical Safety Services knowledge.
  • Understanding of ICH, CIOMS, GVP, and basic pharmacovigilance requirements.
  • Effective communication and teamwork skills.

Responsibilities

  • Manage and develop Patient Safety staff, delegate work according to allocated budgets and hours, and coordinate resource assignments and staffing needs with appropriate leaders.
  • Guide day-to-day team performance, create development plans, provide coaching and training, conduct appraisals, and address performance concerns.
  • Ensure assigned work meets Service Level Agreements and defined Key Performance Indicators for quality, compliance, and training.
  • Provide functional expertise and oversight for Patient Safety processes, respond to team queries, and support urgent workload requirements when needed.
  • Execute Patient Safety activities aligned with team objectives, implement resource utilization plans, and contribute to process improvement and continuous improvement initiatives.
  • Maintain current knowledge of relevant regulations and client and Parexel Standard Operating Procedures, and support audits, inspections, quality investigations, risk mitigation, and response activities.
  • Manage project budgets and resource allocation, forecast resource needs, track performance metrics, manage client expectations, and identify potential scope changes for escalation.
  • Maintain professional client interactions, participate in client and team meetings, address feedback and concerns, and provide periodic project updates to Senior Management.
  • Coordinate team activities, review and validate timesheets, communicate key decisions and policies, support team cohesion, and collaborate with cross-functional teams.
  • Participate in the implementation and optimization of pharmacovigilance automation tools and digital solutions, support team adoption through training, and analyze automated process performance.
  • Assess emerging technologies, recommend improvements to safety workflows, and contribute to innovation roadmaps that enhance efficiency and compliance.
  • Provide technical input for business development activities and support the preparation of materials and presentations as requested.

Desired Qualifications

  • Familiarity with pharmacovigilance process improvements, automation tools, and digital solutions.
  • Knowledge of pharmacovigilance audit and inspection requirements.
  • Understanding of project budget management, resource allocation, and resource forecasting principles.
  • Awareness of automation and artificial intelligence applications in pharmacovigilance.

About the Company

Parexel

End-to-end clinical trials and regulatory consulting

Parexel provides end-to-end clinical development services for pharmaceutical, biotechnology, and medical device clients from Phase I to Phase IV. Its offerings include clinical trial management, regulatory consulting, and biostatistical analysis to support the design, execution, and analysis of clinical studies. The company operates as a CRO, partnering with sponsors to manage trials, ensure regulatory compliance, and generate robust data for drug development. What sets Parexel apart is its breadth of services across the trial lifecycle, emphasis on quality and reliability, and industry recognition, along with a focus on patient-centric approaches and leadership in gender partnership. The company’s goal is to help clients bring new therapies to market efficiently and safely by delivering high-quality, compliant trial outcomes and data that support regulatory submissions.

Company size
10,001+
Company stage
Acquired
Total funding
$8.5B
Headquarters
Durham, NC
Founded
1982

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