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Job DescriptionAbout MMS MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS maintains a 97 percent customer satisfaction rating. Our mission is to deliver high-quality service and technology solutions – rooted in strong science and decades of regulatory experience – that will assist our clients in developing and marketing life-changing therapies to positively improve lives worldwide. MMS recognizes that a talented staff is what drives our business forward. Identifying and attracting top talent and continual training to strengthen core skills are essential to its core mission. At MMS, enthusiasm, collaboration, and teamwork are fostered, knowing that a global and diverse talent pool makes the company stronger. For more information, visit www.mmsholdings.com or follow MMS on LinkedIn. Responsibilities • Under minimal supervision, the Medical Writer will critically evaluate, analyze, and interpret the medical literature to select primary resource materials for adequate study design, statistical significance, scientific rigor and absence of bias, • Write and edit clinical development documents, including but not limited to, clinical protocols, investigator’s brochures, clinical study reports, subject consent forms, integrated safety and efficacy summaries, Module 2.7.1, 2.7.2, 2.7.3, 2.7.4, and 2.5 documents, presentation materials and publications to medical journals, • Complete writing assignments in a timely manner, • Maintain timelines and workflow of writing assignments, • Practice good internal and external customer service, • Highly proficient with styles of writing for various regulatory documents, • Expert proficiency with client templates & style guides, • Interact directly and independently with client to coordinate all facets of projects; competent communicator skills for projects, • Contribute substantially to, or manages, production of interpretive guides, • Take ownership of a given assignment, proactively consulting other project team members and other department representatives for information or guidance as necessary, • Mentor medical writers and other members of the project team who are involved in the writing processRequirements, • At least 3 years of previous experience in the pharmaceutical industry, • Must have at least 3-5 years of industry regulatory writing and clinical medical writing experience, • The ideal candidate would hold a Bachelors, Masters, or Ph.D. in scientific, medical, clinical discipline, • Substantial clinical study protocol experience, as lead author, required, • Experience leading and managing teams while authoring regulatory documents with aggressive timelines, • Experience in regulatory submissions (clinical study reports) presented to regulatory authorities a plus, • Understanding of clinical data, • Exceptional writing skills are a must, • Excellent organizational skills and the ability to multi-task are essential prerequisites, • Candidate must be an expert in MS Word, Excel, PowerPoint, and related word processing tools, • Experience being a project lead, or managing a project team, • Strong understanding of federal regulations, Good Clinical Practices, and ICH guidelines a plus, • Not required, but experience with orphan drug designations and PSP/PIPs a plus Powered by JazzHR GKlKQ2pvlh

Job DescriptionDescription: Description: We are seeking a highly skilled Legislative Affairs and Policy Analyst to provide comprehensive support for legislative monitoring, policy analysis, and strategic communication. This position is contingent upon contract award. This role serves as a key resource for tracking congressional activity, preparing high-level briefings, and translating complex scientific and programmatic information for internal and external stakeholders. The successful candidate will be a proactive researcher and writer capable of supporting the organization’s engagement strategy with legislative bodies and senior management. Key Responsibilities: • Monitor, track, and analyze legislative proposals and actions daily, providing technical feedback and research to support organizational policy initiatives., • Draft responses to inquiries from legislative staff, research services, and oversight bodies, and assist in preparing testimony and responses to questions for the record., • Prepare high-quality presentation materials, fact sheets, and narratives that translate complex programmatic and budgetary data for non-scientific audiences., • Support the annual budget process by drafting and vetting potential questions and answers to ensure consistent messaging., • Assist in the development and execution of annual legislative communication plans and maintain active logs of congressional engagements., • Conduct quarterly assessments of the impact of new or revised legislation on organizational operations and policy priorities., • Serve as a subject matter expert, providing training on congressional procedures and communication protocols to internal program and laboratory staff., • Maintain a deep understanding of organizational services and activities to provide effective, informed support to leadership., • Meet regularly with internal stakeholders to establish priorities, assess performance, and align communication strategies with organizational goals., • Assist with the planning and execution of congressional site visits, including on-site logistical and communications support.Requirements:, • Bachelor’s degree in environmental studies, marine affairs, marine biology or related., • Minimum of 4 years of demonstrated experience in legislative affairs, policy analysis, or government relations within a NOAA mission-driven environment/contract., • Exceptional ability to distill complex technical/scientific information into clear, persuasive, and accurate materials for diverse audiences., • Strong understanding of the legislative process, including how to monitor bills, track congressional actions, and prepare formal briefing packages., • Ability to analyze budget data and programmatic impacts, connecting them to high-level policy initiatives., • Ability to interact effectively with senior leadership and external stakeholders with a high degree of discretion and professionalism., • Capacity to manage multiple competing deadlines in a fast-paced "quick response" environment., • Excellent verbal communication and training skills, with the ability to explain complex congressional procedures to non-experts., • Willingness and ability to travel as needed to support congressional engagements and training sessions. Compensation: Competitive salary and benefits package commensurate with experience. If you are a motivated individual with a passion for continuing your work with NOAA, we want to hear from you! @Orchard is an equal opportunity employer. We encourage all qualified candidates to apply, regardless of race, gender, age, disability, or other protected characteristics.

Following our successful expansion into the U.S. and continued growth across Europe, we are seeking a Medical Writer to help drive our Scientific function from our Austin or Barcelona hubs. Reporting directly to our Chief Scientific Officer, this person will play a critical role as the medical voice behind Aika, ensuring that what we build, publish, and communicate is grounded in sound medical science, clinical best practice, and patient-centric thinking. The focus is on hands-on scientific writing, publications, and content. Who We're Looking For: A scientifically trained professional with strong writing instincts and a track record in clinical development, medical affairs, medical writing, or scientific communications. We're looking for someone who can hold the medical pen on high-stakes documents and, at the more senior end, represent Biorce credibly with KOLs, sponsors, and regulators. This person should be able to combine sharp scientific judgment with clear, compelling writing: producing everything from peer-reviewed publications to medical input on product workflows. Key Responsibilities: • Produce high-quality scientific outputs: peer-reviewed publications, white papers, value dossiers, conference materials, and other written deliverables that strengthen Aika's credibility., • Contribute to medical and scientific input on Aika's core clinical functionalities, including protocol design support, eligibility logic, and endpoint frameworks., • Partner with Product and Commercial teams to ensure AI models and workflows reflect current standards of care, clinical guidelines, and regulatory considerations., • Translate complex clinical and scientific concepts into clear, accurate, and engaging content for different audiences (sponsors, KOLs, internal teams, external publications)., • Act as a scientific voice for Biorce externally: supporting advisory boards, scientific conferences, and strategic partner discussions., • Shape the medical and therapeutic direction of the platform, prioritizing work that addresses real-world challenges in drug and device development. Requirements Must-haves • Advanced scientific or clinical background: life sciences, pharmacy, medicine, or related (a medical degree, PharmD, or clinical PhD is required)., • Experience in clinical development, medical affairs, medical writing, scientific communications, or a related function in pharma or biotech., • Solid understanding of clinical trial methodology, endpoint selection, and benefit-risk assessment., • Excellent scientific writing skills with a portfolio of published or client-facing work., • Strong stakeholder management skills and high integrity. Nice-to-Haves • Experience working with or overseeing digital health and AI-driven platforms., • Exposure to multiple therapeutic areas or indications., • Experience presenting at scientific conferences or sitting on advisory boards., • Hands-on experience with protocols, eligibility criteria, endpoints, or regulatory documents. Why Join Us? • A dynamic work environment with an international team, where collaboration and diversity thrive., • Work alongside top talent, united by a shared purpose and committed to making a real impact., • Comprehensive private health coverage to ensure your physical and mental well-being., • Hybrid work model offering flexibility to balance your professional and personal life., • Company events to celebrate achievements and enjoy time together., • Get equipped with a MacBook to enhance your productivity and work experience., • Our office is pet-friendly! You'll likely be greeted by a few wagging tails upon arrival.

Research, write, edit and proofread complex technical data.Create, maintain and update manuals, procedures, specifications and other documents.Create, maintain and update installation instructions, training material and other technical documents.Design and establish style guidelines and standards fo

Job Overview We are seeking a Technical Writer responsible for creating clear, concise, and comprehensive documentation that communicates complex technical concepts related to our autonomous surface vessels. Responsibilities * Collaborate with engineers, designers, and other stakeholders to gather

Content Writer Job Duties: Writing Take podcast episodes and turn them into amazing blogs, LinkedIn posts, and show notes that flatter our clients and their guests.

Senior Technical Writer Employment Type: Full-Time, Experienced Department: Technology Support CGS is seeking an experienced Senior Technical Writer to provide consultative, analytical, and documentation support for a large Federal agency initiative.

Find us on Instagram: @optimizely Introduction A skilled Technical Writer to help create the content users need, when and where they need it. Soft Skills: Perform peer reviews for other writers, writing for style and concision.