Methods is a £100M+ IT Services Consultancy who has partnered with a range of central government departments and agencies to transform the way the public sector operates in the UK. Established over 30 years ago and UK-based, we apply our skills in transformation, delivery, and collaboration from across the Methods Group, to create end-to-end business and technical solutions that are people-centred, safe, and designed for the future. Our human touch sets us apart from other consultancies, system integrators and software houses - with people, technology, and data at the heart of who we are, we believe in creating value and sustainability through everything we do for our clients, staff, communities, and the planet. We support our clients in the success of their projects while working collaboratively to share skill sets and solve problems. At Methods we have fun while working hard; we are not afraid of making mistakes and learning from them. Predominantly focused on the public-sector, Methods is now building a significant private sector client portfolio. Methods is part of the Global Alten Group.

• Leading UK teleradiology company established in 2013 • Founded by Professor Sujal Desai and Professor Simon Padley renowned cardiac and thoracic radiologists with a distinguished background at the Royal Brompton Hospital • The opportunity to work in your own time and in your own space! • An excellent work-life balance • Incentives for high-volume reporters • User-friendly cloud-based PACS/reporting technology • Your worklists matched to your skills (The Right Radiologist for the Right Study at the Right Time) • Outstanding clinical leadership

• Leading discovery sessions to understand business needs and translate them into OnePlan configurations • Implementing and integrating PPM or Work Management platforms such as OnePlan, Microsoft Project Online, or Smartsheet • Configuring portfolios, project plans, resource plans, and financial tracking to support strategic prioritization and delivery • Using Microsoft technologies such as Project, Power BI, Power Automate, and Microsoft 365 to extend solutions and connect with client ecosystems • Partnering with clients throughout the delivery lifecycle from requirements gathering through adoption • Delivering workshops, demos, and presentations that show clients the possibilities of their solutions • Managing solution rollouts in a remote setting while keeping stakeholders engaged and informed

Title: Regulatory Affairs Consultant- R&D Location: Guelph United States Job Description: At Elanco (NYSE: ELAN) - it all starts with animals! As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets. At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose - all to Go Beyond for Animals, Customers, Society and Our People. At Elanco, we pride ourselves on fostering a diverse and inclusive work environment. We believe that diversity is the driving force behind innovation, creativity, and overall business success. Here, you'll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights. Making animals' lives better makes life better - join our team today! Supervisor Title: Director, US Regulatory Affairs Job Level: P3 Position Type: Full Time Job Function: Regulatory Affairs Location: USA/Canada Your Role: Regulatory Affairs Consultant- R&D Represent the Regulatory US Affiliate to ensure regulatory compliance and timely submissions for post-approval regulatory activities related to assigned pharmaceutical (FDA-CVM) products and/or areas of responsibility. Additionally, demonstrate leadership by providing innovative solutions, promoting a positive work environment, and effectively communicating to ensure delivery and maintenance of Elanco's food animal and pet health pharmaceutical portfolio. Your Responsibilities: - Maintain a broad overview of all post-approval activities related to assigned products and/or areas of responsibility. - Provide regulatory guidance in the development and approval of promotional materials for the Elanco US Affiliate to support the food animal and pet health marketed pharmaceutical products and new launches. - Support post-approval label changes, CMC updates, periodic reports and other post-approval submissions to FDA-CVM. This may include but is not limited to compilation, submission and archival. - Lead project teams to comply with non-standard post-approval requests and authority mandates. - Collaborate with other functional areas (Global CMC, Marketing, Legal, Technical, Labeling, Supply Chain, Quality, etc.) and external partners to promote regulatory awareness of and compliance with applicable regulations and internal policies and procedures. - Represent Elanco in direct communications with FDA-CVM, in written form and by leading meetings as required by the project. - Maintain positive business collaboration and influence with Elanco Reg Affiliates, Reg Innovation, FDA-CVM and industry groups. - Perform other related duties and assignments as required by the business and directed by management. What You Need to Succeed (minimum qualifications): - Master's degree or equivalent with at least 5 years relevant work experience within the sciences or related areas. - Solid understanding of US FDA-CVM regulatory post-approval requirements - Strong ability to interpret and leverage scientific data for promotional purposes while maintaining compliance with regulations. What will give you a competitive edge (preferred qualifications): - Experience with promotional material/technical material review in the FDA/EPA space. - Self-management skills in an environment with diverse needs and demanding, and often urgent, timelines - Demonstrated ability to collaborate across organizations and develop compliant solutions that meet the needs of all parties. - Strong oral and written communication skills and attention to detail Additional Information: - Domestic and international travel, up to 5% - Location: Global Elanco Headquarters - Indianapolis, IN - Hybrid Work Environment Don't meet every single requirement? Studies have shown underrepresented groups are less likely to apply to jobs unless they meet every single qualification. At Elanco we are dedicated to building a diverse and inclusive work environment. If you think you might be a good fit for a role but don't necessarily meet every requirement, we encourage you to apply. You may be the right candidate for this role or other roles! Elanco Benefits and Perks: We offer a comprehensive benefits package focusing on financial, physical, and mental well-being while encouraging our employees to pursue our purpose! Some highlights include: - Multiple relocation packages - Two weeklong shutdowns (mid-summer and year-end) in the US (in addition to PTO) - 8-week parental leave - 9 Employee Resource Groups - Annual bonus offering - Flexible work arrangements - Up to 6% 401K matching Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status Elanco may use automated tools, including AI, to support parts of our recruitment process, such as reviewing applications against job‑related criteria and/or transferrable skills. These tools help ensure a consistent, structured evaluation, but they do not make hiring decisions. All decisions involve a human reviewer.