Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $3B in revenue in our last fiscal year with extensive growth potential ahead. At the heart of Veeva are our values: Do the Right Thing, Customer Success, Employee Success, and Speed. We're not just any public company – we made history in 2021 by becoming a public benefit corporation (PBC), legally bound to balancing the interests of customers, employees, society, and investors. As a Work Anywhere company, we support your flexibility to work from home or in the office, so you can thrive in your ideal environment. Join us in transforming the life sciences industry, committed to making a positive impact on its customers, employees, and communities. The RoleWe are looking for an experienced Senior Consultant with deep expertise in navigating customers through complex software implementation. Veeva’s Vault RIM suite is the industry’s only unified software solution that provides fully integrated regulatory information management (RIM) capabilities, including data and document management, submission publishing, and archival on a single cloud-based platform. As a key member of our Professional Services team, the Senior Consultant will be responsible for understanding our customers’ global regulatory needs, translating requirements into solution design, and defining global strategies for deploying our cloud-based solution for managing regulatory information across the enterprise. There is no work location requirement (remote position) within the EU/UK if a candidate is in close proximity to an airport and able to meet travel requirements. Qualified EU/UK based candidates are encouraged to apply. What You'll Do - Lead software implementation projects at life sciences companies ranging from the world's largest pharmaceutical companies to emerging biotechs - Lead the solution design for implementation and use of the Vault Regulatory suite (Veeva Registrations, Veeva Submissions, Veeva Submissions Archive, Veeva Publishing) - Lead configuration requirements workshops, design, prototype, configure, and document content solutions - Program and project management, including resource planning, leading and motivating a cross-functional team - Primary customer liaison managing communication between the project team, customer, and internal stakeholders - Mentor project team and consultants, helping others improve their consulting skills Requirements - 8+ years experience performing system implementations for life sciences or healthcare companies, either as a consultant, business or IT representative - In-depth knowledge of drug development processes and regulatory submissions; including, Labeling, Submission Publishing and/or Viewing systems - Proven ability to collaborate and communicate excellently with diverse stakeholders and ensure delivery to a high degree of satisfaction - Influential; experience leading teams through hard decisions and negotiating compromises - Technical abilities and willingness to “roll up your sleeves” to design, configure and implement a RIM solution - Expert on life sciences compliance and computer systems validation requirements - Ability to work independently in a fast-paced environment - Ability to travel as required by the business Nice to Have - Direct experience with systems such as Veeva Vault, PAREXEL/ LIQUENT InSight, CSC Regulatory Tracker, ArisGlobal Register, OpenText, SharePoint, Documentum, FirstDoc/FirstPoint, NextDocs, CARA, Salesforce, Workday, Oracle, SAP, Lorenz Docubridge, Extedo eCTD Manager, Master Control, Trackwise, other regulatory information management or submission publishing systems, etc. - Consulting experience, working with a major system integrator or software vendor - PMP certification - Execution experience with Agile methodology and/or ACP Certification - SaaS/Cloud experience - Fluency in one or more of the following languages: German, French, Spanish, Italian Interviewing with Veeva We value your time and believe in a transparent hiring process. Here is the process you can expect. - Follow the application process and submit your resume. - Within 3 days, you will receive a link to a personality assessment administered by a third party. - Once you complete the assessment, our team will review your full application package and follow up via email with our decision. - If moving to the interview stage, the process is as follows: - A conversation with the hiring manager - A practical case exercise - A final conversation with our group's Senior Leader. - Once all interviews are complete, the manager will be in touch with a final decision. Compensation - Total compensation: 90,000 - 150,000 EUR - The total compensation range listed here has been provided to comply with local regulations and represents a potential total compensation range for this role. Please note that actual total compensation may vary within the range above or below, depending on experience and location. We look at compensation for each individual and base our offer on your unique qualifications, experience, and expected contributions. This position's total compensation may be composed of other types of compensation, such as variable bonus and/or stock bonus. #LI-Remote #LI-MidSenior Veeva’s headquarters is located in the San Francisco Bay Area with offices in more than 15 countries around the world. As an equal opportunity employer, Veeva is committed to fostering a culture of inclusion and growing a diverse workforce. Diversity makes us stronger. It comes in many forms. Gender, race, ethnicity, religion, politics, sexual orientation, age, disability and life experience shape us all into unique individuals. We value people for the individuals they are and the contributions they can bring to our teams. If you need assistance or accommodation due to a disability or special need when applying for a role or in our recruitment process, please contact us at talent_accommodations@veeva.com.

Role Description NeoGenomics has an opening for a Privacy Specialist I operating Remotely who wants to continue to learn in order to allow our company to grow. The Privacy Specialist I supports the organization's privacy program through monitoring, auditing, investigation support, patient rights administration, education, and compliance activities. Working under the direction of the Privacy Manager, this role assists with maintaining compliance with HIPAA and other applicable privacy laws while helping foster a culture of privacy and compliance throughout the organization. Core Responsibilities: - Assist with privacy risk assessments and support remediation efforts for identified risks - Provide support for privacy initiatives and annual compliance work plan activities - Update and collaborate on privacy policies, procedures, and training to ensure ongoing compliance with evolving regulatory requirements - Assist staff with handling requests for patient information and processing other legal/regulatory requests as needed - Assist with the investigation of potential or actual breaches of protected health information (PHI) and other privacy-related data; assist in the development and implementation of corrective action plans for identified issues and coordinate applicable follow-up with action plan owners - Conduct routine monitoring and auditing to assess the organization’s compliance with privacy requirements; partner with appropriate departments and individuals to resolve noted findings - Process and track requests for Accounting of Disclosures, Amendments of PHI, and Requests to Restrict Use and Disclosure - Coordinate and track business associate inventory - Assist with maintaining a data inventory for new and existing products, services, and business processes - Analyze trends of key performance indicator results for performance improvement opportunities - Analyze privacy metrics and identify opportunities for process improvement - Draft and distribute reports weekly, monthly, quarterly, and annually - Continually improve and update knowledge to accommodate changes to the organization’s regulatory environment and needs Position Objectives: - Demonstrates sound judgment and escalates matters appropriately - Successfully manages assigned work and priorities to meet deadlines - Communicates effectively with employees at all levels of the organization - Collaborates effectively with Compliance, Legal, Information Security, Human Resources, and Operational teams - Maintains confidentiality and professionalism when handling sensitive information - Works productively and efficiently to achieve company and departmental goals - Adheres to NeoGenomics Laboratories core values and safety and compliance policies Qualifications - Bachelor’s Degree (preferably in a healthcare related field) or equivalent work experience required - 1+ year of experience in healthcare compliance, privacy, health information management, healthcare operations, risk management, laboratory operations, or a related field preferred - Working knowledge of HIPAA Privacy Rule requirements and healthcare privacy principles - Familiarity with healthcare compliance programs and regulatory requirements - Strong organizational, analytical, and problem-solving skills - Ability to manage multiple priorities, projects, and deadlines, as well as adapt to changing business needs - Strong written and verbal communication skills - Ability to maintain confidentiality and exercise discretion when handling sensitive information - Ability to participate in team projects and fill various roles such as team member, facilitator, or leader as needed - Experience reviewing, organizing, and tracking compliance data and documentation - Proficiency with Microsoft Office applications, particularly Word, Excel, and PowerPoint - Familiarity with healthcare technology systems such as EHRs, laboratory information systems, or incident management systems preferred Benefits - Highly competitive benefits with a variety of HMO and PPO options - Company 401k match - Employee Stock Purchase Program - Tuition reimbursement - Leadership development - 16 days of paid time off plus holidays - Wellness courses - Highly engaged employee resource groups

• Primary Installation Role responsibility where location of work may vary across the United States. • Collaborate and partner with Sales, Project Manager, Network Design and Digital services, customer IT and biomed to implement solutions sold. • Use technical knowledge to install, monitor, and customize clients' systems after an initial purchase of hardware or software. • Ensure a client doesn't only buy a product but has a positive experience with it. • Assess and remediate existing infrastructure to support installation of new solution. • May also perform installation, validation, and connectivity on assigned equipment. • Function as co-lead; develop and maintain strong relationships and frequent communications with customers and sales to proactively identify customer needs, ensure resolution, proper follow-up, and ongoing customer satisfaction. • Consulting with IT and biomed on customer requirements for installation and address cyber security concerns. • Mentoring and coaching local FE on installed solution. • Responsible for prompt administrative responsibilities such as maintaining customer service logs and internal service records in a timely manner, technical project plans, technical walk thru and post warranty conversations with customer. • Manage vendor service as needed. • Provide instruction to personnel on equipment operation, diagnostics, effective use, and repair. • Supports engineering new product releases.

Role Description As a Sr Implementation Consultant on our Professional Services team, you will be a key contributor to the digital transformation of healthcare across Manitoba. This role is central to successfully rolling out our Electronic Medical Records (EMR) to various ambulatory clinics and healthcare institutions across the province. You will be trained to deploy numerous Altera applications, with a primary focus on the Sunrise EMR Core and Ambulatory functionalities, including related products such as DBmotion, CPM, Opal, and Patient Portal. In addition, you will provide expert workflow consulting services by following a structured methodology through all phases of the implementation life cycle. Your efforts will directly ensure the successful and seamless implementation and utilization of our solutions, moving clinics from paper-based to fully electronic platforms. Responsibilities - Implement the full suite of Altera software solutions, with emphasis on our Sunrise EMR (Core and Ambulatory), at our client sites, primarily in Manitoba. - Perform all project workplan tasks in accordance with contracted project scope, functioning as a vital member of a larger project team (including PMs, Solution Architects, Clinical Consultants, and CMIOs). - Perform complex system configuration tasks, including providing high-level consultation and technical guidance on system configuration to clients. - Provide expert workflow consultation and guidance to clients on critical ambulatory processes, including registration, scheduling, and clinical documentation. - Proactively identify, resolve, and/or escalate system and complex workflow issues that arise throughout your implementation project. - Provide comprehensive activation support; consistently meet or exceed client utilization and transformation targets. - Set appropriate expectations with various client stakeholders, from end-users to executive leadership (e.g., CMIOs), and expertly manage them throughout the project life cycle. - Anticipate client needs, function as a client advocate, and demonstrate exceptional stakeholder engagement skills to foster successful project delivery. Qualifications - Bachelor’s degree or equivalent years of experience required. - 2+ years of hands-on healthcare IT implementation and configuration experience. - Strong, demonstrated functional knowledge of an EMR/EHR system. - Specific expertise in Altera Sunrise EMR (Core or Ambulatory) is preferred. - Experience with Epic or Meditech is also valued if coupled with deep knowledge of essential clinic workflows (e.g., registration, scheduling, clinical documentation). - Must have experience working as part of a formal implementation project team that has successfully rolled out EMR systems. - Clinical background preferred (SME who has rolled out clinics). - Technical background, i.e. background in SQL or SSRS reporting preferred. - Proven client presentation experience; strong written and oral communication skill set, with the ability to communicate effectively with diverse stakeholders (technical resources to executive leadership). - Project management experience; skilled at managing numerous key priorities simultaneously during a long-term (e.g., 12-month) implementation cycle. - History of taking on roles, tasks, and projects where quickly learning new information is required; a "quick study." Requirements - 10-15% travel. Travel is primarily to provide critical on-site support during final go-live activities. - Remote role. Candidates may live anywhere in US. - Candidates located in the U.S. will be considered if they possess the skill set required, have a valid passport and are willing to travel to Canada as required. Benefits - Salary Range: $75,000 - $85,000 USD. - The salary range reflects the anticipated base salary for this position at the time of posting. - Final compensation may vary based on factors including experience, skills, education. Company Description Altera, a member of the N. Harris Computer Corporation family, delivers health IT solutions that support caregivers around the world. These include the Sunrise™, Paragon®, Altera TouchWorks®, Altera Opal, STAR™, HealthQuest™ and dbMotion™ solutions. At the intersection of technology and the human experience, Altera Digital Health is driving a new era of healthcare, in which innovation and expertise can elevate care delivery and inspire healthier communities across the globe.