Job Description

Direct message the job poster from Master Compliance Director of Recruitment & Sales - Pharma, Lifesciences & Medical Devices Role: Global Pharmacovigilance Safety Systems Consultant Location: Remote Position Overview: We are seeking an experienced Global Pharmacovigilance (PV) Safety Systems Consultant to support the design, implementation, and ongoing maintenance of global safety databases and related PV systems. This role plays a critical part in ensuring our pharmacovigilance infrastructure remains compliant, efficient, and aligned with regulatory requirements. Key Responsibilities: Provide both strategic guidance and hands-on support for the design, deployment, and maintenance of PV systems including, but not limited to, Veeva Safety , Veeva SafetyDocs , Rave Safety Gateway , and Commonwealth Vigilance Workbench . Collaborate closely with internal IT teams, external vendors, and PV stakeholders to ensure system validation, upgrades, and data migrations are conducted in full compliance with regulatory standards and business objectives. Conduct business needs assessments and provide project management support for PV system initiatives. Develop and maintain line listings and safety reports to support safety data analysis and signal detection activities. Prepare and maintain comprehensive project and validation documentation for PV systems. Coordinate and execute User Acceptance Testing (UAT) for system enhancements or new deployments. Perform system administration tasks, including user access provisioning and updates. Qualifications: Minimum 8 years of experience working with safety databases and PV systems. Bachelor’s degree (or higher) in Life Sciences, Information Technology, Engineering, or a related field. Demonstrated expertise in one or more PV Safety Databases (e.g., Oracle Argus , Veeva Safety ), including system implementation, data migration, and day-to-day operations. Proven experience in integrating safety databases with other enterprise systems via gateways. Strong analytical and problem-solving skills with a keen attention to detail. Solid understanding of global PV regulations and compliance frameworks (FDA, EMA, ICH). Excellent written and verbal communication skills, with the ability to collaborate across cross-functional teams and influence at all organizational levels. Experience in continuous process improvement within a global pharmacovigilance environment. Global work experience and ability to work effectively across time zones preferred. Willingness to travel occasionally as required. Ideal Candidate Attributes: Systems-thinker with a strategic mindset and strong project management capabilities. Proactive, adaptable, and aligned with core organizational values such as Patients First , Action , Unconventional Thinking , Talent , and Integrity . Seniority level Seniority level Mid-Senior level Employment type Employment type Contract Job function Job function Project Management and Management Industries Biotechnology Research and Pharmaceutical Manufacturing Referrals increase your chances of interviewing at Master Compliance by 2x Get notified about new Drug Safety Specialist jobs in Massachusetts, United States . Vice President, Drug Safety and Pharmacovigilance Boston, MA $325,000.00-$360,000.00 1 day ago Executive Director, Head of Pharmacovigilance Clinical Trial Associate/Sr. Clinical Trial Associate Associate Director, Pharmacovigilance Operations Specialist/ Senior Specialist, Clinical Quality Assurance Associate Director, Pharmacovigilance Training & Compliance Boston, MA $153,600.00-$241,340.00 2 weeks ago Vice President, Head of Safety & Pharmacovigilance Senior Director, Drug Safety and Pharmacovigilance Cambridge, MA $132,000.00-$165,000.00 2 weeks ago Burlington, MA $132,000.00-$165,000.00 2 weeks ago Director, Drug Safety & Pharmacovigilance Scientist Boston, MA $260,000.00-$390,000.00 4 weeks ago Associate Director, Pharmacovigilance Quality Assurance Associate Director, Global Pharmacovigilance Quality Management We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI. #J-18808-Ljbffr Master Compliance

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