- Hackensack Meridian Health (Hackensack, NJ)
- …our mission to transform healthcare and serve as a leader of positive change. The ** Medical Writer Clinical Trials ** is responsible for analyzing, ... implementing comprehensive workflows and project planning to ensure ongoing clinical trial compliance across the Disease Specific...Higher Education Degree (MS, PhD, MD). + Knowledge of clinical trials and the regulation (local, state,… more
- Abbott (Plymouth, MN)
- …our rapidly growing clinical team within the EP division. The Medical Writer will be responsible for producing abstracts, manuscripts, scientific ... colleagues serve people in more than 160 countries. **Senior Medical Writer ** **Working at Abbott** At Abbott,...Minimum of 5+ years of related work experience in clinical trials / medical writing + Cardiovascular… more
- Sanofi Group (Morristown, NJ)
- …accelerate progress. The Principal Medical Writer is a key member of the Medical Writing team, the Clinical Trial Team (CTT) and Project Team. This ... **Job Title:** Associate Director-Principal Medical Writer **Location:** USA, Remote. Proximity...regarding both the project as a whole, and individual clinical studies. **Our Team:** Global Medical writing… more
- Stryker (Fremont, CA)
- Stryker is currently seeking a **Staff Medical Writer ** to join our Neurovascular Division to be based in Fremont, CA or remotely anywhere within the United ... States. **What you will do** As **Staff Medical Writer ,** you will work closely with...evidence from multiple sources such as current and past clinical trials , post-market clinical follow… more
- IQVIA (Durham, NC)
- …avoir une bonne maitrise des outils informatiques. **Job Overview:** Acts as Lead Medical Writer on most types of writing projects. Prepares assigned documents ... a protocol or report. + Good understanding of common statistical methods used in clinical trials and/or interpretation of their results. + Ability to effectively… more
- IQVIA (Durham, NC)
- **Job Overview:** Acts as Lead Medical Writer on any type of writing project, including projects with multiple deliverables/components. Prepares assigned ... inconsistencies in documents. + Good understanding of common statistical methods used in clinical trials and/or interpretation of their results. + Ability to… more
- University of Colorado (Aurora, CO)
- …development and manufacture of novel biologics and cell therapies for early phase human clinical trials . The Gates Biomanufacturing Facility is one of the core ... **Quality Control Analyst I Data Reviewer/Technical Writer ** **Description** **University of Colorado Anschutz Medical...facilities or clinics operated by our affiliated hospital or clinical partners or by CU Anschutz, you will be… more
- ICON Clinical Research (Raleigh, NC)
- …you will play a pivotal role in crafting compelling and accurate proposals for clinical trials and research projects, ensuring they meet client requirements and ... clinical development. We are currently seeking a Proposals Writer II to join our diverse and dynamic team....disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation… more
- Houston Methodist (Houston, TX)
- …cycle of a cure from conceptual bench research, to prototyping and development, to clinical trials and FDA approval. The Research Institute supports more than ... At Houston Methodist, the Scientific Writer position is responsible for performing a variety...performing a variety of tasks including preparing laboratory and clinical studies and documents for submission to journals and… more
- Houston Methodist (Houston, TX)
- …cycle of a cure from conceptual bench research, to prototyping and development, to clinical trials and FDA approval. The Research Institute supports more than ... The Houston Methodist Peak Brain & Pituitary Tumor Center seeks a scientific writer . The scientific writer will primarily be responsible for proofreading and… more
- Ascendis Pharma (Princeton, NJ)
- …across time zones. + Ability to understand, interpret and communicate data from clinical trials . + Proven ability to work with and lead cross-functional, ... mission of developing new and potentially best-in-class therapies to address unmet medical needs. Our culture fosters a place where skilled, adaptable, and highly… more
- NTT DATA North America (Highland Heights, KY)
- …accuracy, and regulatory compliance of laboratory instruments and software systems used in clinical trials . This role requires a strong technical background in ... Software Validation Analyst with 6-9 years of progressive experience in the clinical research, pharmaceutical, or biotechnology industry to join their team in… more
- University of Utah (Salt Lake City, UT)
- …**Job Summary** The Research Compliance Office Data Manager will ensure data for oncology clinical trials is accurate, complete and entered in a timely manner, ... team including the Principal Investigator (PI), Biostatistician, and Protocol Writer . This position will be responsible for developing, validating,...CCRP , CCRC , or CCRA ). + Oncology clinical trial experience preferred. + Working knowledge… more
- UCLA Fielding School of Public Health (Los Angeles, CA)
- …whole body MRI, as well as gain expertise in standardized response assessment of clinical trial imaging. Fellows will also participate in the PET/CT and PET/MR ... UCLA Position overview Position title: Oncology Imaging Fellow/Health Sciences Clinical Instructor Salary range: The posted UC salary scales… more