Medical Writer Salary at Dna Comms BETA

About This Role TFS HealthScience is a leading global, mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and functional service (FSP) solutions. The Medical Writer / Technical reviewer will be responsible for the scientific accuracy, data and referencing quality, appropriate style, and correct branding of scientific/medical assets for the sponsor globally. Also will work in an international and cross-functional environment, following global and local guidelines and working closely with internal and external stakeholders to ensure the highest quality for the sponsor assets and gathering data on asset quality and agency performance. Key Responsibilities Perform data/referencing quality check of scientific/medical assets; ensuring all content is scientifically accurate and appropriately supported by the Reference Docum

Job Title: Medical Writer, Immuno-Oncology Location: Waltham, MA (On-Site) 3-4 months Contract - (chance to extend based on project) JOB DESCRIPTION: Overview: Our client is a small Boston-based clinical-stage biotechnology company dedicated to developing next-generation immunotherapies for cancer and autoimmune diseases. Leveraging deep expertise in biologics, the company designs proprietary biotherapeutics with tissue- and cell-specific targeting, bispecific formats, and novel masking technologies for precision drug delivery. They are seeking a Medical Writer to support a Pre-IND submission and related documentation for a first-in-class immunotherapy program targeting solid tumors. This contract role will focus on authoring and reviewing regulatory documents, research manuscripts, and technical summaries in collaboration with R&D leadership and external partners. The position reports directly to the EVP of R&D and will work closely with scientific leads, project management, and exter

Senior Medical Writer, Medical Communications Job Summary Our Senior Medical Writers work as part of a multidisciplinary team (including medical director, editor, graphic designers, and account personnel) to produce slide decks, infographics, web-based and social media materials, meeting reports, strategic communications platforms, medical publications, and other materials requiring sound clinical judgment and excellent writing skills. Senior Medical Writers work on multiple projects simultaneously and manage their workload under strict timelines. They are responsible for developing content that supports therapeutic areas & product positioning of pharmaceutical, biotech & medical device clients. Level of experience and ability to effectively partner with medical directors to create efficiencies justifies the senior role. Essential Duties & Responsibilities Participating as an active team member in providing strategic recommendations and contributing to continuous quality improvement De

_________________________________________________________________________________: Applied Medical is a new generation medical device company with a proven business model and commitment to innovation fueled by rapid business growth and expansion. Our company has been developing and manufacturing advanced surgical technologies for over 35 years and has earned a strong reputation for excellence in the healthcare field. Our unique business model, combined with our dedication to delivering the highest quality products, enables team members to contribute in a larger capacity than is possible in typical positions. Position Description: Collaboration is a fundamental part of our organization's culture and is essential to our continued success. As such, the successful candidate for this position is expected to work on-site, enabling them to engage fully with colleagues and contribute to cross-functional initiatives. Therefore, the ability to work collaboratively and contribute to a positive an

TFS HealthScience is a leading global, mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and functional service (FSP) solutions. Scientific Communications Medical Writer About This Role The Medical Writer will support the development and maintenance of global medical information content, including writing and formatting, documentation, reporting and metrics on global Medical Information activities. The Medical Writer will work under the guidance of the Scientific Communications Manager in regard to content and timelines and adhere to defined client standards as well as safeguard that processes and system standards are followed. Key Responsibilities Production of new global standard scientific response content (gSSRC) as defined by the Scientific Communications Manager and in accordance with the client Medical Inform

Medical Writer – Immuno-Oncology Location: Waltham, MA (On-site) Contract: 12 months (Potential to Extend) A growing clinical-stage biotech company is seeking an experienced Medical Writer to support the preparation and submission of regulatory and research documentation within the immuno-oncology space. This individual will collaborate with R&D and functional leads to draft, edit, and review key documents including INDs, Investigator’s Brochures, clinical study reports, and manuscripts. Responsibilities: Draft high-quality PIND/IND documents and research manuscripts Translate complex immuno-oncology data into clear regulatory content Coordinate review cycles and lead quality control for submissions Ensure consistency and compliance with ICH/FDA standards Develop and maintain documentation systems and templates Qualifications: MS required; PhD preferred 8–10+ years of medical/scientific writing experience Strong understanding of immunology or immuno-oncology data Proven ability to mana

Planet Pharma's client is looking for an Associate Director / Senior Medical Writer, who will be responsible for providing medical writing support for the development of complex clinical documents for regulatory submissions including, but not limited to clinical protocols, informed consents (ICFs), clinical study reports (CSRs), investigator brochures (IBs), patient narratives, annual reports and other key clinical and regulatory documents. This individual will support the overall strategy for all medical writing processes according standards. Key Accountabilities/Responsibilities: Manage medical writers (in-house FTEs and contractors, and external vendors) who are individually contributing to the MW activities for a variety of regulatory documents Author clinical content and project manage SME contribution of regulatory documents to develop content for regulatory submissions that is well-organized, consistent, accurate, and that complies with applicable company SOPs, style guide, lexi

Medical Writer, Immuno-Oncology Company: Cugene Inc. Location: Waltham, MA (On-site) Position Type: 1-Year Consultancy (with possibility of extension) ABOUT US Cugene is a Boston-based clinical-stage biotechnology company dedicated to developing next-generation immunotherapies for cancer and autoimmune diseases. With deep expertise in biologics, we use advanced molecular modeling and precision engineering to create proprietary biotherapeutics featuring tissue- and cell-selective targeting antibodies in bispecific and multifunctional formats, along with novel masking technologies for targeted drug delivery. We seek high-performing team members who are skilled, proactive, and solutions-oriented individuals who take initiative, embrace challenges, and are motivated to advance new therapies. At Cugene, employees contribute directly to shaping R&D, translational and clinical strategies, working collaboratively to move innovative science from the lab into the clinic. ROLE DESCRIPTION To supp