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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in leading cross-functional transformation projects within Global Pharmacovigilance, focusing on process optimization, data governance, and compliance with GxP requirements. Proficient in implementing Veeva Safety and driving digital transformation initiatives in regulated environments.
Highest-signal resume keywords
Pharmacovigilance OperationsVeeva Safety ImplementationsAgile/Lean Six Sigma/PMP MethodologiesData GovernanceRegulatory Compliance
Tech Stack
Tools & technologiesAbout the role
Key responsibilities & impact- Lead cross-functional transformation and innovation projects across Global Pharmacovigilance
- Drive continuous improvement initiatives to optimize PV processes, safety workflows, and system performance
- Support enhancement and post-implementation optimization of Veeva Safety and related business processes
- Define project scope, deliverables, timelines, and KPIs, and monitor progress
- Translate business needs and operational challenges into process improvement and digital transformation initiatives
- Develop and strengthen PV data governance frameworks
- Promote data quality, integrity, and standardization
- Ensure compliance with GxP requirements, regulatory expectations, and internal quality standards
- Identify, assess, and implement automation and AI-driven solutions
- Partner with Digital Technology teams, Veeva, and external vendors to design, validate, and deploy tools in regulated environments
- Liaise between business and technical stakeholders
- Facilitate change management, stakeholder alignment, and adoption of new processes and technologies
Requirements
What you’ll need- Master's degree in Life Sciences, Pharmacy, Biomedical Sciences, Information Systems, or a related discipline
- 7–10 years of experience in Pharmacovigilance, PV systems, business transformation, pharmaceutical consulting, or related areas
- Proven track record of leading cross-functional projects within global pharmaceutical or highly regulated environments
- Strong expertise in pharmacovigilance operations, safety databases, regulatory requirements, and GxP compliance
- Hands-on experience in Veeva Safety implementations, PV transformation programs, Agile/Lean Six Sigma/PMP methodologies, and collaboration with technology partners and digital teams
- Solid knowledge of data governance, data integrity, quality management, and process optimization methodologies
- Experience translating business needs into functional, operational, and technology-driven solutions
- Understanding of digital transformation, AI, automation, and innovation opportunities in regulated environments
- Excellent project leadership, stakeholder management, communication, and problem-solving skills, with the ability to manage multiple priorities independently
Benefits
Comp & perks- Opportunity to work at Excelya, a health company and mid-size CRO
- One-stop provider service model offering full-service, functional service provider, and consulting projects
- Diverse project opportunities
- Working alongside preeminent experts
- Employee experience-focused environment
- Opportunities to contribute to scientific, operational, and human knowledge
- Environment that values natural talents and nurtures professional potential
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Project LeadershipProcess OptimizationSafety WorkflowsData IntegrityQuality ManagementAutomation SolutionsAI-Driven SolutionsDigital TransformationStakeholder ManagementKPI Monitoring
Soft Skills
CommunicationProblem-SolvingChange ManagementCollaborationStakeholder Alignment
Tools & Technologies
VeevaSafety DatabasesDigital Technology ToolsRegulated Environments
Industry Keywords
Pharmaceutical ConsultingGxP ComplianceLife SciencesBiomedical SciencesPharmacy