The Senior Medical Writer may require a bachelor's/master's degree. Responsible for researching, writing, and editing clinical/statistical reports and study protocols: summarizes data from clinical studies for submission to the Food and Drug Administration (FDA). Being a Senior Medical Writer typically reports to a supervisor or manager. Working as a Senior Medical Writer typically requires 4 to 7 years of related experience. Contributes to moderately complex aspects of a project. Work is generally independent and collaborative in nature.
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When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. ...
When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. ...
Position. We are seeking an experienced, detail-oriented individual to work with our Medical Writing team. In the Senior Medical Writer role, you will be responsible for independent lead authoring and editing of medical and regulatory writing deliverables that support the clinical portfolio. You will partner with colleagues within Medical Writing as well as with the Nonclinical, Clinical, & Regulatory teams to prepare high-quality, accurate and c...
Position. We are seeking an experienced, detail-oriented individual to work with our Medical Writing team. In the Senior Medical Writer role, you will be responsible for independent lead authoring and editing of medical and regulatory writing deliverables that support the clinical portfolio. You will partner with colleagues within Medical Writing as well as with the Nonclinical, Clinical, & Regulatory teams to prepare high-quality, accurate and c...
Overview. Develops high-quality documentation that address laboratory testing technology, test selection, and test interpretation. Writes, edits, and/or reviews design control documents, abstracts, posters, and scientific manuscripts for publication at professional meetings or in peer-reviewed journals. Manages Design Control in vitro diagnostic (IVD) development documentation using validated document control systems providing technical expertise...
Responsibilities. The Senior Medical Writer is responsible for crafting and editing clinical and scientific documents, including statistical analysis summaries, literature reviews, abstracts, and posters, for regulatory submissions or sponsor use. Key duties include. Collaborating with sponsors and/or internal medical personnel and statisticians to develop clinical development plans, study protocols, and clinical study reports. Designing template...
PROMETRIKA is a full-service clinical research organization (CRO) with extensive experience in clinical operations, data management, biostatistics, medical writing, and pharmacovigilance. We’re driven by our passion for the human aspect of our work and our compassion for the people whose lives have been improved by the innovations we help bring to market. Our clients include national and international biopharmaceutical and medical device companie...
Synterex. Inc. is a. global. consortium of highly experienced clinical development professionals specializing in medical writing, submission publishing, and clinical science and operations support. Synterex. offers remote or on-site services, with a focus on providing clear, concise. accurate. and fully compliant documentation, from early drug development through post-approval. . Synterex. is. seeking. an organized, motivated, and collaborative i...
Senior. Medical Writer. Responsibilities. Independently write and lead the development of Clinical Study Reports (CSRs), including CSR Shells (Sections 1-9), Key Messages Map, and CSR Statistical Text (Results only - Sections 10, 11, and 12). Closely interact with statisticians and other team members in the development of key messages map and CSR statistical text. Drive the document preparation process, draft and distribute documents for review, ...
DESCRIPTION. Training Communications Healthcare. Are you a versatile writer who thrives on creating diverse educational materials for a range of audiences. Do you have a passion for life sciences, learning and development, and communications. If you're driven by making things happen and eager to learn, our team is looking for strong collaborators, effective communicators, and detail-oriented professionals. We are searching for a senior medical wr...
Sr Medical Writer/Sr. Publications Specialist. HM's Top 3. Medical writing within a clinical research context (e.g. scientific, peer reviewed manuscripts reporting on primary or secondary outcomes). Experience in medical device or pharmaceutical company. Experience with cardiac rhythm concepts or general cardiology experience. Education Required: Bachelor’s. Years’ Experience Required: 4 years medical writing or related field (or 2 years with adv...
Company Description. A Few Words About Us. Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty aretas: Information Technology (I...
