• Develop and implement software solutions according to technical requirements, ensuring appropriate quality and performance • Participate in defining solution architectures, always seeking the best technical approach • Code, test, and maintain systems, applying best practices and coding standards • Conduct code reviews, promoting continuous improvement and compliance with established standards • Collaborate with other teams (analysts, testers, etc.) to ensure effective system integration • Identify issues and develop effective solutions, ensuring system stability and efficiency • Keep technical system documentation up to date, including usage instructions and architecture • Perform unit tests and ensure systems meet quality and performance requirements • Contribute to the continuous improvement of tools, processes, and methodologies used in development • Support training and mentoring of less-experienced developers • Stay up-to-date with market trends, suggesting technological innovations applicable to the development environment

• Own and lead the deployment, integration and commissioning of data center building automation controls systems • Recommend and enforce controls and monitoring standards in new and existing data center projects • Manage 3rd-party vendors to ensure timely delivery of data center automated controls • Partner with construction, commissioning, operations and field engineering • Finalize and implement Controls Normalization Plans ServerFarm’s data center fleet

• Own the end-to-end technical onboarding experience for new enterprise customers, from kickoff through successful integration • Build and maintain integration scripts, tooling, and documentation to accelerate customer time-to-value • Serve as the primary technical point of contact during the onboarding phase, translating customer requirements into actionable engineering solutions • Diagnose integration issues across customer environments (APIs, data pipelines, cloud infrastructure) and drive them to resolution • Collaborate closely with product and engineering to surface customer feedback and influence the roadmap • Develop reusable onboarding playbooks and internal tooling to scale the deployment process • Travel to customer sites occasionally for critical onboarding milestones or technical workshops

Role Description The Site and Monitoring Health Lead (SMH Lead) will apply knowledge of regulations and GCPs as well as experience in monitoring to safeguard the quality of clinical trial execution at investigator sites and ensure the client’s oversight of CRO monitoring effectiveness. This is a site-facing position that reports to the FSP Manager, with work directed by the client Associate Director (or above), Site and Monitoring Health Team. Key Accountabilities - Oversight of monitoring effectiveness - Implements various types of oversight encounters and activities as applicable including but not limited to: - Site risk analysis - Site contacts - Aggregate review of data - Monitoring visit report review - Sponsor Oversight Visits - System/data spot checks - Periodic summaries - Ensure timely documentation of these activities is completed and filed - Completes Sponsor Oversight Visit reports consistently on time and with good quality - Utilizes a risk-based approach to review critical to quality items at the site level and study level, exhibiting an “inspection ready at all times” mentality - Creates Study Specific Oversight Plans (SSOPs) for aligned trials in scope and/or follows SSOP when conducting oversight activities - Troubleshoots and uses alternative and innovative approaches to solve problems impacting clinical site delivery and quality - Utilizes root cause analysis to assess identified issues and provide suggested actions to Study Management/Clinical Research Organization (CRO) to mitigate risk - Supports inspection preparation and management Collaborative Relationships - Works both independently and collaboratively with cross-functional teams - Builds relationships with investigators and site staff in region; acts as a resource for identifying potential sites for new studies - Supports investigator sites less experienced in research; assists in assuring sites are engaged in the study and have what they need to recruit participants successfully - Works closely with Clinical Risk and Analytics staff to understand the risk management plan (Risk MAP) for assigned studies, ensures the SSOP is aligned with the Risk MAP, and assesses sites who are outliers Operational - Implements client Site and Monitoring Health strategy in alignment with applicable International Council for Harmonization-Good Clinical Practices (ICH-GCP) regulations - Leads oversight and trend meetings with the study team and/or Clinical Research Organization (CRO) to discuss risks, issues, and trends identified by the SMH team for the trial - Remains current with global regulatory requirements, has a current working knowledge of local/regional regulatory requirements Qualifications - Ability to think innovatively and be willing to initiate changes, introduce new ideas, and creatively problem-solve - Ability to build and maintain relationships with key investigators and sites (e.g. key networks, key trial sites and investigators, key opinion leaders and their site staff) - Ability to analyze complex situations and effectively communicate issues along with potential recommendations to various functional groups - Demonstrates good judgment and decision-making experience - Ability to travel; moderate, may include local or regional - Demonstrates flexibility in schedule and willing to travel frequently in assigned region - Good organizational skills and ability to deal with competing priorities - Effective interpersonal verbal, written and presentation communication skills - Proficient with MS Office Suite (Excel, Word, and PowerPoint); able to learn internal and external computer systems - Proficient in written and spoken English required; proficient in local language, as applicable, preferred; fluent in multiple languages and cultural awareness preferred Knowledge and Experience - Significant direct monitoring experience gained with a CRO or pharmaceutical company working on multinational clinical studies - Previous CRO monitoring oversight experience and experience with oversight visits required - Lead CRA experience required - Experience in all study phases of clinical research (Phase I-III) - Previous audit and regulatory inspection experience preferred - Ability to travel; moderate travel EEO Disclaimer Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.