When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.
Key Accountabilities:
Technology Support
Conduct and drive set-up and support activities associated with the Parexel safety database (and associated systems) including but not limited to:
New study set-up
Periodic report configuration and generation
Ad-hoc report configuration and generation
Expedited report rule configuration
End-user support
Drive and support the planning and delivery of the handover of the safety database from client to Parexel were contracted to take over the pharmacovigilance tasks for complex client projects
Drive and support the planning and delivery of the handover of safety data from Parexel to client at the end of study/project as contracted for complex client projects
Provide the authorship and reviewer roles for standard operating procedures and controlled documents that pertain to safety technology
Design and deliver complex integration solutions between Parexel safety technologies and other applications to drive operational excellence, enhanced service capabilities
Organizational Representation
Represent Safety Technology Management and the safety operations organization and be directly responsible for actions when interfacing with other Parexel groups (such as TQM, QA, IT) to ensure that database, hardware, network, security, quality, integration, support and project services associated with maintained systems are adequate and sufficiently managed
Represent Safety Technology Management and the safety operations organization and be directly responsible for actions when interfacing external auditors and inspectors during the examination of safety technology
Develop and deliver presentations for the service delivery of Parexel safety technology solutions
Issue Management
Lead collaboration with Parexel IT, vendor, Parexel Safety Services staff, and clients for the proper analysis, resolution, and closure of issues for supported systems
Team Support
Train and coach new or developing staff in the systems and activities necessary for the fulfillment of their job responsibilities
Provide work direction to team members in the execution of their duties for daily operational support and strategic implementation services
Change Management
Lead and drive change management in accordance with the Software Development Life Cycle through the ownership of activities including impact assessments, testing methodologies, and qualification.
Lead and drive software updates, change requests and application support for the supported applications
Lead, design and drive the implementation of technology solutions for Safety Services for the purposes of business process optimization and improvement
Ensure adherence to regulations concerning computer system validation, 21 CFR Part 11 compliance, procedures, and quality standards
Collaborate with Global Pharmacovigilance Intelligence Office to ensure Parexel safety systems maintain regulatory compliance and proactively meet requirement as they change
Skills:
Advanced interpersonal, verbal, and written communication skills
Client focused approach to work
Advanced analytical and problem-solving skills
Advanced organizational and customer service skills
Willingness to work in a matrix environment and to value the importance of teamwork
Drive and support a team working through problem management. Own at least one solution.
Take ownership of core tasks related to the support and maintenance of safety technologies
Advanced level experience in System Administration and application support skills within pharmacovigilance safety technology, including complex configurations and client-specific solutions for safety databases, gateway / E2B, report development, signal detection
Knowledge of emerging pharmacovigilance safety technology, including AI
Advanced level skills in using standard scripting languages e.g., SQL
Experience of industry standard Service Desk Tools
Advanced level technical writing capability
Advanced experience of standard SDLC processes including change management
Advanced experience of Agile methodology
A flexible attitude with respect to work assignments and new learning
Drive and complete multiple and varied tasks with enthusiasm and prioritize workload for others using standard Project Management methodologies
Advanced experience of system validation and change management
Advanced knowledge and practical application of computer system regulations and guidance in the pharmaceutical industry including: 21 CFR Part 11, EMA Annex 11, GAMP
Advanced knowledge of Pharmacovigilance roles, standards and practices
Advanced knowledge of GVP and GCP
Knowledge and Experience:
Safety Supportive Applications (Argus, Vault Safety, EDC, Safety ERP) - 5+ years of experience in all functional areas of chosen safety technology including all secondary tools and processes
Safety Business Processes - 5+ years of experience working closely with operational teams to manage issues, gather and document requirements, and deliver solutions
Peer oversight, coaching, training - 1+ years of direct mentorship or training
Propose and Deliver System/Process Improvements - Demonstratable lead participation in improvement initiatives
System Validation Activities - 1+ years in design, execution, maintenance activities and their documentation
Communication Skills - Strong, Fluent in English; demonstrated ability to write technical documentation and deliver clear presentations to stakeholders and clients
Leadership Representation - 1+ years as a point of contact and directly responsible individual working with cross-functional teams as a safety technology representative
Fluent in Japanese: demonstrated ability to communicate with Japan internal resource and clients to manage issues, gather and document requirements, and deliver solutions.
Education:
BA/BSc Engineering/Computer Science, Masters or equivalent preferred
Parexel is a leading global clinical research organization (CRO) providing insights-driven Clinical and Consulting solutions to the world’s life sciences industry. Leveraging deep local knowledge and a global breadth of clinical, regulatory and therapeutic expertise, our 24,000+ professionals worldwide work in partnership with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind — broadening access and making clinical research a care option for anyone, anywhere. Our proven track record spans 40+ years and drives us forward, advancing clinical research in healthcare’s most complex areas while harnessing innovation to drive efficiencies across every phase of the clinical development process. Our insights-driven approach, proven delivery and trusted execution are accelerating the delivery of life-changing treatments to patients — With Heart.™ We continue to earn recognition industrywide, including the 2025 Scrip Award for “Best Contract Research Organization – Full-Service Provider,” 2024 Fierce Biotech CRO Award for "Innovative Approaches to Patient-Centric Research" and the 2024 and 2023 Society for Clinical Research Sites (SCRS) Eagle Award.
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