Senior Medical Writer

Join Integrated Resources, Inc. as a Medical Writer, where you will play a pivotal role in the development of high-quality medical documentation. In this dynamic position, you will collaborate with cross-functional teams to produce regulatory documents, clinical study reports, and other materials that adhere to industry standards.

Join Integrated Resources Inc. as a Medical Writer, where your expertise will contribute to the advancement of healthcare communications. In this role, you will create and edit high-quality scientific documents, ensuring clarity and compliance with regulatory standards. Collaborate with cross-functional teams to produce materials that effectively convey complex medical information.

Join our team as a Medical Writer III, where you will play a vital role in creating and maintaining high-quality medical documentation. You will collaborate with cross-functional teams to ensure that all materials meet regulatory and compliance standards. Your expertise will contribute to the advancement of medical information and communication within our organization.

As a Principal Medical Writer at Sobi, you will leverage your expertise in communication to spearhead a strategy-oriented approach in crafting pivotal clinical and regulatory documents. Your role will be crucial in ensuring clarity, credibility, and consistency of clinical information across submission packages and clinical programs, thereby facilitating regulatory assessment and achieving product labels that meet commercial needs.Key Responsibilities:Lead an effective strategy for authoring clinical components of regulatory submissions, ensuring that the scientific content is clear, concise, complete, credible, and compelling, aligned with regulatory document objectives.Take the lead in preparing essential clinical and regulatory documents, including those that support major regulatory submissions and responses to regulatory agencies/health authorities.Provide leadership and project coordination to cross-functional authoring teams, ensuring timely delivery, high quality, and compliance with regulatory standards for clinical documents.Collaborate with senior project staff to develop a storyboard for submissions and plan document development to optimally support the proposed prescribing information.Serve as a Product Medical Writer, offering strategic medical writing expertise and support across multiple projects within a clinical development program.Ensure that all documents meet high technical quality standards in accordance with in-house technical requirements.Mentor and develop less experienced Medical Writers.Oversee and coordinate the contributions of all Medical Writers involved in documents under your purview, including in-house consultants and Medical Writers at Contract Research Organizations (CROs).

Artech Information Systems LLC is seeking a highly skilled Medical Writer III to join our dynamic team in Cambridge. As a pivotal member of our organization, you will craft and develop high-quality scientific documents that support our clients' clinical and regulatory needs. This role demands a meticulous approach to research and an ability to translate complex scientific data into clear, concise narratives.

We are seeking a highly skilled and motivated SOP Writer III to join our dynamic team in Cambridge. The ideal candidate will play a crucial role in developing and refining standard operating procedures (SOPs) that ensure operational excellence across the organization. This is an exciting opportunity to contribute to the success of our projects through meticulous documentation and process improvement.

We are seeking a highly skilled SOP Writer III to join our dynamic team. In this role, you will be responsible for developing and refining Standard Operating Procedures (SOPs) that adhere to industry regulations and ensure operational excellence. The ideal candidate will possess a keen eye for detail and a strong understanding of technical writing principles.

Your Contribution at Lila Lila Sciences is in search of a skilled and knowledgeable Technical Science Writer / Content Creator to play a pivotal role in articulating our scientific endeavors. This position resembles that of a managing editor, where you will convert intricate scientific concepts into precise and comprehensible content, while also mentoring a select group of contract writers to maintain exceptional storytelling quality. This role is crucial as impactful science can only transform the world when it is both understood and trusted. Your contributions will assist: Customers in grasping what Lila enables, its functionality, and its reliability. Partners in identifying opportunities for collaboration and understanding effective integration. Government and public-sector partners in evaluating relevance, safety, and societal benefits. Investors in comprehending the technical advantages, platform strategy, and long-term vision. Future employees in recognizing our ambitions, rigorous standards, and the challenges they will tackle. Your Responsibilities Draft and refine high-quality articles, explainers, technical summaries, case studies, and multimedia scripts that convey complex scientific themes with precision and narrative strength. Produce content that links what we are developing to its significance, emphasizing scientific integrity, measurable outcomes, and responsible communication. Targeted Storytelling Customize messaging and formats to meet the diverse needs of stakeholders: Customers: practical results, workflows, reliability, and real-world constraints. Partners: collaborative roadmaps, innovation narratives, and integration stories. Government entities: public benefits, validation, safety, and responsible use. Investors: distinctiveness, defensibility, and platform direction. Candidates: our mission, culture of rigor, and the problems they will address. Develop “layered” content assets, allowing a core story to be adapted across various formats (e.g., social media posts, blogs, technical briefs, presentations). Editorial Leadership Delegate tasks to contract writers, establish clear guidelines, and provide constructive feedback to ensure quality, coherence, and a consistent voice.

Costello Medical is hiring an IT Administrator based in Cambridge, England. This position plays a central role in keeping the company’s IT infrastructure stable and secure, supporting the daily work of teams across the business. Key responsibilities Maintain and oversee IT systems throughout the organization Troubleshoot technical issues, including both hardware and software problems Apply solutions to improve system performance and strengthen security Role focus This role centers on supporting smooth operations by resolving IT challenges and ensuring reliable technology for colleagues. Company mission Costello Medical provides medical communications and data analysis services. The IT Administrator helps support this mission by making sure technology works efficiently and securely.

Join our team at Integrated Resources Inc. as a Technical Writer, where you will play a crucial role in crafting and refining documentation that supports our innovative projects. You will collaborate closely with engineers, product managers, and other stakeholders to ensure that complex technical concepts are conveyed clearly and effectively. Your expertise in writing and editing will help us maintain high standards of quality in our documentation.

Join us at Jobs for Humanity as we seek passionate Speakers and Writers who are ready to inspire and empower diverse communities. Your words can make a difference, driving social change and promoting inclusivity. We value creativity, originality, and the ability to engage audiences effectively.

Role SummaryResponsibilities: You will play a pivotal role in enhancing the company’s commercial operations and business development initiatives while supporting our objective of establishing enduring strategic partnerships with our clients.Salary: £24,500 to £26,000 per annum, commensurate with your experience.Benefits: Enjoy discretionary profit-sharing bonuses disbursed biannually, flexible working arrangements, a generous holiday allowance, private medical insurance, critical illness coverage, income protection, and full sponsorship for external training opportunities. For more details, visit our benefits page.Role Type: Available as either full-time or part-time, permanent roles.Start Date: We are looking for candidates who can start in April or May 2026; please indicate your availability in your application.Application Deadline: Submit your application by Friday 8th March 2026. We will conduct interviews shortly after this date.Location: This opportunity is based at our Global Headquarters in Cambridge.About the RoleAt Costello Medical, a globally recognized B Corp certified medical communications firm, we are experiencing rapid growth driven by our unwavering commitment to exceptional customer service and high-quality deliverables. To facilitate this expansion, we seek a motivated Business Administrator to become part of our dynamic and collaborative External Engagement team.In this capacity, you will assist in various administrative tasks related to our business development and commercial processes, including:Commercial & Negotiation SupportAssisting in the administration of commercial negotiations within the pharmaceutical and healthcare industries by preparing necessary materials, compiling historical communications, and coordinating essential documents.Utilizing Excel to create pricing documents (rate cards) by extracting data, calculating new rates, and drafting proposals.Maintaining and updating commercial data in our internal systems.Overseeing the management of the team’s shared inbox, responding to inquiries, directing requests to appropriate team members, and ensuring timely communications.Coordinating and supporting regular team meetings focused on commercial topics, including scheduling, agenda preparation, note-taking, and action item circulation.Business Development SupportAssisting in business development initiatives and campaigns for our client-facing teams.Conducting research on client pipelines and facilitating outreach efforts to enhance engagement.

Your Contribution at Lila Sciences At Lila Sciences, we believe that scientific discoveries only make a meaningful impact when they are effectively communicated. Our Government sector team acts as a vital link between exceptional researchers and the government clients and internal stakeholders who rely on their insights. We are on the lookout for a Physical Science Technical Writer who excels in this pivotal role. In this role, you will report to the Head of Government Partnerships and act as a crucial connector between our scientific team and the stakeholders who support and implement their research findings. You will take complex technical information, methodologies, and data and translate them into clear, credible, and actionable language. Collaborating closely with our Grants Manager, who oversees the proposal process, you will craft the technical and scientific elements that lie at the core of successful submissions. As a quality assurance gatekeeper, you will leverage your domain expertise to identify scientific inaccuracies, challenge vague claims, and ensure that all deliverables adhere to the highest standards of technical excellence before they are finalized. This position transcends mere documentation maintenance; it is a strategic communication role designed for someone with enough scientific acumen to grasp intricate research concepts and the communication prowess to convey them to non-specialist audiences. Importantly, we seek a candidate who is adept at utilizing AI tools as a productivity enhancer: a writer who can harness LLMs, create streamlined automation processes, or design workflow tools that empower individuals to achieve remarkable outcomes. Key Responsibilities Translate Scientific Research for Government StakeholdersEngage directly with Lila's scientists and engineers to fully comprehend their research, then generate briefings, white papers, and executive reports that effectively communicate scientific insights to government clients, program officers, and agency stakeholders, adjusting tone, depth, and format as needed. Proposal and Grant Development SupportCollaborate with the Grants Manager to create the technical and scientific components of proposal applications (technical narratives, methods descriptions, scientific appendices) for initiatives funded by the DOE and UK, ensuring consistency in tone, format, and compliance throughout. Content Repository and Knowledge ManagementDevelop and maintain a repository of reusable, version-controlled technical content, including vetted scientific descriptions, methods summaries, capability statements, and regulatory narratives, to facilitate efficient knowledge transfer.

Join our dynamic team at Integrated Resources Inc. as a skilled Medical Coder. In this pivotal role, you will be responsible for accurately translating healthcare services into standardized codes used for billing and insurance purposes. Your attention to detail and coding expertise will play a crucial role in ensuring proper reimbursement and compliance within the healthcare system.

About BlueRock TherapeuticsBlueRock Therapeutics LP is a pioneering clinical-stage company focused on innovative cell therapies aimed at addressing neurological and ophthalmic disorders. Our leading investigational therapies, bemdaneprocel (BRT-DA01) for Parkinson’s disease and OpCT-001 for primary photoreceptor diseases, are at the forefront of clinical development. Established in 2016 as a collaboration between Versant Ventures and Leaps by Bayer, BlueRock embodies a culture defined by resilience, urgency in transforming healthcare, integrity in our mission, and a sense of community that emphasizes our collective purpose.Our VisionWe are harnessing advanced scientific techniques to guide the differentiation of universal pluripotent stem cells into authentic, functional cells, paving the way for allogeneic cellular therapies that can tackle a wide range of diseases. Our commitment to cellular and gene therapy is shaping the future of medicine and providing hope through new therapeutic options for countless patients.We are looking for talented individuals who thrive in a collaborative environment, embrace a dynamic workplace culture, and are dedicated to advancing innovative cellular therapies that will significantly impact patients' lives.The Director of Medical Writing will offer strategic and operational leadership across all Medical Writing initiatives to support BlueRock’s project portfolio from early development stages through to product registration.This role will be responsible for establishing and managing a cohesive Medical Writing function that produces high-quality regulatory documents in alignment with BlueRock’s global strategy, development timelines, and corporate objectives. The Director will lead an internal medical writing team, oversee vendor collaborations, and act as a key strategic partner to various departments including Regulatory Affairs, Pharmacovigilance, Clinical Development, Clinical Operations, Biometrics, Translational Science, and Technical Operations. Additionally, this role will play a crucial part in evolving capabilities such as AI-enabled medical writing, content reuse strategies, and collaborative models with Bayer teams.

The Opportunity: Join Relay Therapeutics as a Senior Medical Director, where you will be pivotal in propelling our clinical pipeline from IND to proof of concept and ultimately to registration. In this role, you will partner with senior medical staff to shape clinical strategies, design clinical trials, and ensure successful execution. Collaborating across various functions including clinical project management, regulatory affairs, clinical operations, biostatistics, data management, and medical writing, you will significantly contribute as Relay Therapeutics continues to advance product candidates into clinical settings. You will provide clinical leadership to R&D teams and closely collaborate with Development leadership. We are open to remote employees

Join our dynamic team as a Medical Information Associate II where you will play a pivotal role in providing accurate and timely medical information support. This is an excellent opportunity for entry-level professionals eager to start their career in the healthcare industry. You will be responsible for responding to inquiries, ensuring compliance with company policies, and contributing to the overall efficiency of our medical information services.

Alkeus Pharmaceuticals, Inc. is a pioneering clinical-stage biotech company dedicated to developing innovative therapies for severe ocular diseases with significant unmet medical needs. Located in the vibrant city of Cambridge, Massachusetts, Alkeus was established in 2010 and has since made strides in advancing its leading compound, gildeuretinol acetate (ALK-001). Recognized as a breakthrough therapy and awarded orphan drug status by the U.S. Food and Drug Administration, gildeuretinol is currently under investigation in multiple clinical trials aimed at treating Stargardt disease and geographic atrophy (GA) secondary to age-related macular degeneration (AMD), which is a leading cause of blindness in the United States.Position Summary:We are on the lookout for a dynamic and accomplished leader to join our organization as the Vice President of Medical Affairs. This pivotal role will entail guiding the global strategic direction and operational execution of Medical Affairs activities related to our clinical programs in retinal diseases. The VP of Medical Affairs will spearhead a cross-functional medical organization that includes Patient Advocacy, Medical and Scientific Communications, Medical Directors, Medical Operations, Medical Information, and Field Medical (MSLs). By collaborating closely with Clinical Development, Regulatory, Commercial, and other internal and external functions, this leader will ensure scientific excellence in stakeholder engagement, evidence generation, medical communications, and support for phase 3 trials. This individual will also represent the medical perspective in senior leadership forums within the company and to external stakeholders when necessary. Furthermore, they will cultivate and lead a well-structured medical affairs team that effectively supports patient communities.

Join Alkeus Pharmaceuticals, a pioneering biopharmaceutical company dedicated to transforming the lives of patients with rare diseases. We are seeking a dynamic and visionary Medical Director to lead our clinical development activities, providing strategic direction and oversight for our innovative programs.As the Medical Director, you will collaborate with cross-functional teams, engage with key opinion leaders, and contribute to the development of cutting-edge therapies. This is an exceptional opportunity for a dedicated professional looking to make a significant impact in the field of rare diseases.