Role Description We are currently seeking a dedicated Clinical Specialist (Radiation Therapist) to join our Global Standards and Content team. In this role, you will play a key part in educating and supporting new users on our proprietary healthcare oncology software and hardware system products. Working closely with product managers, sales, and marketing teams, you will contribute to developing and delivering training strategies for Siemens Healthineers products. Training and Support: - Strategize, coordinate, and facilitate innovative training solutions for hardware products: TrueBeam, IDENTIFY, and Halcyon. - Act as the primary interface between GCS (clinical), Product Marketing and Product Management, ensuring seamless global communication and data dissemination to internal and external customers. Collaboration with Cross-functional Teams: - Collaborate with Product Managers, Product Engineers, Product Marketing, Curriculum Developers, Information Technologists, Internal/External Trainers, and Instructional Designers to develop comprehensive training strategies and materials (documents and/or videos) for internal and external customers worldwide. Training Coordination: - Coordinate and lead customer and employee training classes, with a focus on innovative training solutions. - Provide demo support at local, regional, national, and global customer trade events. - Conduct large group presentations at seminars, training programs, and trade shows. Content Development and Support: - Prepare comprehensive lesson plans based on engineering documentation, field service requirements, and software documentation to address specific implementation questions. - Formulate complementary support training information, including quick tips, procedures/course manuals, and onsite training documentation. - Utilize video creation tools, with proficiency in Camtasia. - Support team members in the implementation of innovative technologies and training solutions. Qualifications - Experience in radiation therapy or related field. - Strong communication and presentation skills. - Ability to work collaboratively in a cross-functional team environment. - Proficiency in video creation tools. Requirements - Must be able to work with controlled technology in accordance with US export control law. Benefits - Medical insurance - Dental insurance - Vision insurance - 401(k) retirement plan - Life insurance - Long-term and short-term disability insurance - Paid parking/public transportation - Paid time off - Paid sick and safe time

Role Description As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. While this is a remote role, candidates located in the U.S. Eastern Time Zone are preferred to support alignment with clients and business operations. How will you make an impact? - Communication Strategy: Develops and executes a strong communications and content strategy, positioning Thermo Fisher as a top CDMO in the industry. - Market & Competitive Intelligence: Leads market insights and brings perspective to competitive intelligence, while exercising oversight of the Market Intelligence team and their work with key stakeholders. - Content Leadership: Shapes Thermo Fisher’s CDMO thought leadership and voice; develops high-value content marketing strategies that demonstrate our technical acumen, expertise and SME’s. - Leadership: Provides leadership and guidance to their team and ensures high performance. - Strong Collaboration: Team-first mindset when partnering within the Marketing Team, with key stakeholders (leadership, PR team, SME’s, divisions, etc), and externally with agencies, media and vendors. - Media Strategy: Leverage deep understanding of CDMO trade media to create opportunities for Thermo Fisher thought leadership and positioning in the market. How will you get there? - Education: Bachelor’s degree in business, communications or marketing strongly preferred. - Experience: 10-15 years of communications/content experience, required; CDMO experience, required; Strong team player; Strong writing skills. Qualifications - Industry Expertise: Deep experience in the CDMO industry and of the overall drug development process, from early phase through commercialization. - Content Strategy: Expert at creating and shaping content to drive a leadership position in top CDMO journals and publications through paid and earned media. - Content & Communications: Ability to translate complex technical information into compelling messages and relevant content for biotech and biopharma content. - Strategic Thinking: Strong understanding of the CDMO market and business acumen regarding marketing’s role to position and differentiate Thermo Fisher in the market. - Leadership & Influence: Experience leading teams or driving initiatives cross-functionally and without direct authority. - Agency Acumen: Ability to thrive in a fast-paced environment, making quick decisions, and driving teams to deliver high quality work in compressed timelines. Benefits - The salary range estimated for this position based in New Jersey is $170,000.00–$220,000.00. - This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. - We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes: - A choice of national medical and dental plans, and a national vision plan, including health incentive programs. - Employee assistance and family support programs, including commuter benefits and tuition reimbursement. - At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy. - Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan. - Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount.

Role Description - Support Global Study Director (GSD) / Global Study Associate Director (GSAD) and Global Study Managers (GSMs) by completing delegated study work. - Initiate and lead the set-up of the electronic Trial Master File (eTMF). Maintain and close the eTMF to ensure compliance to International Conference of Harmonization Guidelines for Good Clinical Practice (ICH/GCP) and AZ SOPs. - Collaborate with Site Management & Monitoring, extended study team and external vendors in collection of regulatory and other essential documents. - Coordinate regular Quality Checks (QC) and review of the TMF, ensuring continual inspection. - Contribute to electronic applications/submissions by creating and managing clinical-regulatory documents according to the requested technical standards and supporting effective publishing and delivery to regulatory. - Proactively plan and collate the administrative appendices for the CSR. - Initiate and maintain production of study documents, ensuring template and version compliance per study specific requirements. - Set-up, populate and accurately maintain information in tracking and communication tools and support team members in the usage of these tools. - Support the set-up, maintenance and close-out of Clinical Trial Transparency (CTT) activity in PharmaCM, coordinating with relevant stakeholders to fulfil AstraZeneca compliance and meet the regulatory authority needs. - Support the GSD/GSAD with tracking, reconciliation and follow-up of the study budget/payments in relevant systems. - Contribute to application, coordination, supply and tracking of study materials and contribute to collection of study supplies, if required, at the study close-out. - Coordinate administrative tasks and logistic support throughout the conduct of the study, audits and regulatory inspections, according to company policies and SOPs. - Lead the practical arrangements coordination and contribute to the preparation of internal and external meetings (e.g., study team meetings, committee meetings, monitor meetings, Investigator meetings and virtual meetings). Liaise with internal and external participants and/or vendors. Qualifications - Education in medical or biological sciences or discipline associated with clinical research preferred. - Proven organizational and analytical skills. - Previous administrative training/experience. - Computer proficiency in day-to-day tasks. - Develop working knowledge of the Clinical Study Process and an understanding of the range of working procedures relating to it, together with an understanding of the ICH/GCP guidelines. - Excellent verbal and written communication in English. - Demonstrate ability to work independently, as well as in a team environment. - Willingness and ability to train others on study administration procedures. - Global study support experience preferred but not required. - Experience managing eTMF and CTMS systems is required (Veeva Vault experience preferred). Benefits - Various annual leave entitlements. - A range of health insurance offerings to suit you and your family’s needs. - Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. - Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being. - Life assurance. - Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.

Role Description ProGuides is looking for a talented gamer experienced with Voice Over work to host our Fortnite YouTube channel content. The role of host will perform voice overs, and occasional script revisions with talent producer. Host is expected to stay up to date on Fortnite meta, community discussions, and professional tournament standings. Qualifications - Knowledgeable on game mechanics and niche topics - Engages with Fortnite greater community and professional scene - Ability to deliver quality voice overs in a professional and timely manner - Strong understanding and verbal delivery of English language - Past on-camera/VO experience preferred Requirements - Up to date resume - 30 second voice over of this script excerpt (Phone camera/audio): - "Let’s be honest, there’s probably tons of different little things you’re doing wrong in your games, but these five big ones are what really sets you and the pros apart. What’s up Proguides fam, I’m (NAME) and today we’re talking about the top 5 reasons that you might be feeling stuck in your rank. Luckily for you most of these things are easily fixable, so hit that sub button and let’s get into it!" Application Email your audition clip and resume to the email address attached to the Apply button. We look forward to hearing from you!