Role Description Homify is in full expansion in many of our markets, including the Greek-speaking markets for which we’re now looking for Freelance Creative Content Writer in Greek language. Here what you’ll be required to do: - You'll create and write content for our Greek website. - You’ll maintain high-quality standards by implementing our tone-of-voice and expertise across all of your copies. - You'll create engaging articles that resonate with our target audience, keeping an eye on our SEO needs. - You’ll work closely with our content team to provide constructive feedback and review our creative processes. Qualifications - Near-native level Greek. - Relevant experience in writing - journalistic or otherwise creative (experience in appropriate fields beneficial). - Experience with SEO and Proofreading. - Ability to work alone with minimal guidance. - A self-starter mentality is a must. - Good research and proofreading skills. - Strong communication skills. Benefits - Freelance position that can flexibly be performed remote. - Demanding tasks in a fast-growing company. Company Description We are homify - the platform for Home and Living! We offer everything that home lovers need for planning, renovating and decorating their home.

• Write and refine microcopy across the full app: onboarding flows, error messages, paywalls, success screens, empty states, notifications, and more. • Collaborate directly with designers in Figma to address user needs and deliver seamless, intuitive experiences. • Work with POs to understand product goals, user context, and flow logic and translate that into copy decisions. • Apply insights from UX research and user testing to improve clarity and resonance of in-app language. • Maintain and evolve our content style guide to keep voice, tone, and terminology consistent across the product.

Role Description As most of the content provided from field offices are written by people whose native language is not English, copy-editing this content into proper English is extremely important for the Regional Office. The editor will also be expected to make the website as marketable as possible, along with catchy language, titles etc. that would attract the attention of the general population as well as other relevant stakeholders. Under the supervision of the Programme Specialist and Regional Communications Specialist of UN Women ECA RO, the editor will edit the content for the website and UN Women knowledge products, including publications, brochures, briefs, factsheets, guidance documents etc., and ensure the content provided is up-to-date and relevant. The editor may ask for more information, key results, and additional materials. The editor is expected to organize the content in a clear, concise and understandable way, using easy to understand and attractive language when necessary to outreach to larger audiences. - Write/edit/proofread UN Women knowledge products, including but not limited to publications, brochures, briefs, factsheets, policy documents, guidance documents. - Write/edit/proofread web articles for UN Women’s official regional website. - Ensure consistency, accuracy, grammatical correctness and adherence to UN Women’s writing style guidelines. - Liaise with UN Women Programme Specialist, Regional Communications Specialist and other relevant UN Women ECA RO regional staff as well as staff in field offices if needed for review and finalization processes. Qualifications - Master’s degree or equivalent in Communications, Journalism, English, International Relations, Social Sciences or a related field is required. - A first-level university degree in combination with two additional years of qualifying experience may be accepted in lieu of the advanced university degree. Requirements - Minimum 5 years of experience as an editor, writer, with outstanding writing skills. - Extensive experience in creating and editing website content. - Experience in editing materials for human rights-related international organizations. - UN experience is an asset. - Proven record of writing and/or editing in the area of gender equality and women empowerment is an asset. - Record of writing and/or editing in the area of feature stories is an asset. - Excellent analytical skills with strong attention to detail, and ability to work independently under tight deadlines. - Native knowledge of English is required (both written and spoken). Benefits - Payment in full upon final submission and satisfactory outputs/products in accordance with specified requirements. - The time needed to complete all work will be agreed with the ECA RO Programme Specialist prior to being carried out. - The Consultant needs to fill out a timesheet, provided by the ECA RO, that would detail the work that was completed in a day and will be paid based on a daily fee. Company Description In July 2010, the United Nations General Assembly created UN Women, the United Nations Entity for Gender Equality and the Empowerment of Women. The creation of UN Women came about as part of the UN reform agenda, bringing together resources and mandates for greater impact. It merges and builds on the important work of four previously distinct parts of the UN system (DAW, OSAGI, INSTRAW and UNIFEM), which focused exclusively on gender equality and women's empowerment. - At UN Women, we are committed to creating a diverse and inclusive environment of mutual respect. - UN Women recruits, employs, trains, compensates, and promotes regardless of race, religion, color, sex, gender identity, sexual orientation, age, ability, national origin, or any other basis covered by appropriate law. - All employment is decided on the basis of qualifications, competence, integrity and organizational need.

Title: Senior Specialist, Medical Writing, Remote US Locations: USA - California – Irvine USA - Washington - Seattle USA - Arizona – Phoenix USA - Colorado – Denver time type Full time job requisition id Req-44779 Imagine how your ideas and expertise can change a patient’s life. We generate extensive clinical evidence to demonstrate the effectiveness and safety of our innovations and how our products transform patients’ lives. As part of our Clinical Affairs team, you’ll hone your scientific curiosity and passion for evaluating data to increase access to pioneering technologies for patients in need. In close partnership with principal investigators, dedicated medical professionals, patient advocacy groups, and regulatory authorities, you will drive the evidence needed to optimize patient outcomes. Patients with mitral and tricuspid heart valve disease often have complex conditions with limited treatment options. Our Transcatheter Mitral and Tricuspid Therapies (TMTT) business unit is boldly pursuing an innovative portfolio of technologies to address a patient’s unmet clinical needs. It’s our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey. This position is US Remote based. Posting locations are listed for job board tags only. How you will make an impact: - As a key member of the Clinical Science team, the Sr. Specialist, Clinical Science/Medical Writing is responsible for supporting the development of regulatory and clinical documents for a dynamic portfolio of products across TMTT. - Perform and maintain systematic literature searches, developing search terms and criteria, extracting relevant clinical data, and writing clear and concise summaries of the data to support the development of clinical evaluation reports and clinical study reports - Develop routine, sustaining medical writing documents/deliverables; propose approaches to developing moderately complex documents/deliverables - Review and provide thoughtful feedback on moderately complex cross-functional deliverables (e.g., clinical study data, risk management documents, IFUs, SSED) using clinical and technical knowledge - Serve as the primary contact, negotiating deliverables, timelines, and resolving project-related issues with assistance, in collaboration with cross-functional stakeholders - Assist in the implementation of continuous process improvements as it relates to medical writing - Other incidental duties What you’ll need (required): - Bachelor's Degree in a related field with 5 years of related experience working in medical affairs, clinical affairs and/or clinical science or equivalent work experience based on Edwards criteria Required What else we look for (preferred): - Advanced degree (Master’s, PHD, Pharm D) - Experienced with literature reviews and various publication databases including PubMed and Embase. - Experience in authoring clinical evaluation reports - Familiarity with the cardiovascular therapeutic area—including, but not limited to, structural heart interventions, coronary interventions, heart failure—and current treatment landscape; familiarity with clinical research and/or clinical trial experience. - Familiarity with MEDDEV 2.7/1 and EU MDR for clinical evaluations. - Familiarity with FDA PMA applications. - Good knowledge of scientific research methodology, device development process, GCP, ICH guidelines and Global (US FDA, EU MDR) regulations. - Experience working in a cross functional, collaborative environment and comfortable interacting with R&D engineers, regulatory specialists, physicians, statisticians, and support personnel. - Demonstrated ability to work independently, ability to prioritize and manage multiple tasks simultaneously - Excellent oral and written communication skills - Experience with maintaining current, in-depth product knowledge including current developments, clinical literature review, as well as therapeutic and product operation knowledge - Advanced working knowledge with the use of MS PowerPoint, MS Word, MS Excel, EndNote, and Adobe Acrobat - Strong analytical, problem-solving, and scientific writing skills - Strict attention to detail - Ability to interact professionally with all organizational levels - Ability to work in a team environment, including inter-departmental teams and representing the organization on specific projects - Ability to build productive internal/external working relationships - The Sr. Specialist will be an experienced medical device professional with strong scientific acumen and a commitment to putting patients first. Aligning our overall business objectives with performance, we offer competitive salaries, performance-based incentives, and a wide variety of benefits programs to address the diverse individual needs of our employees and their families. For California (CA), the base pay range for this position is $106,000 to $149,000 (highly experienced). The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience). Applications will be accepted while this position is posted on our Careers website. #LI-Remote Edwards is an Equal Opportunity/Affirmative Action employer including protected Veterans and individuals with disabilities. COVID Vaccination Requirement Edwards is committed to protecting our vulnerable patients and the healthcare providers who are treating them. As such, all patient-facing and in-hospital positions require COVID-19 vaccination. If hired into a covered role, as a condition of employment, you will be required to submit proof that you have been vaccinated for COVID-19, unless you request and are granted a medical or religious accommodation for exemption from the vaccination requirement. This vaccination requirement does not apply in locations where it is prohibited by law to impose vaccination.