- Novo Nordisk Inc. (West Lebanon, IN)
- …investigation report contains the technical merit and completeness according to regulatory expectations. The Deviation Investigator- Writer will be responsible ... Are you ready to realize your potential? The Position The Deviation Investigator- Writer is responsible for investigating and writing of deviations to the… more
- Tris Pharma (Monmouth Junction, NJ)
- …with key opinion leaders (KOLs), clinical trial investigators and internal scientific , pharmacology and regulatory teamsReviews data generated during study ... clinical study conduct; Collaborates closely with internal stakeholders, (ie Regulatory Affairs, Product Development, Research and Development (R&D), Quality… more
- Merck & Co. (North Wales, PA)
- …lead clinical scientist on the clinical trial team.Collaborates with the Medical Writer on clinical/ scientific and regulatory documents.Partners with Study ... Job DescriptionThis position drives scientific planning, strategy and execution of Phase 1-4 clinical studies.-Under the direction of the Program Lead, you will… more
- Harvard University (Cambridge, MA)
- Details Title Scientific Writer /Project Manager (Research Associate) School Harvard Medical School Department/Area Department of Microbiology Position ... Description We are seeking a Scientific Writer /Project Manager (Research Associate) to provide...and that documents are error-free and follow formatting and regulatory requirements. * Prepare scientific illustrations; assemble… more
- ThermoFisher Scientific (Juneau, AK)
- …**Senior Medical Writer (North America) (FSP; Remote)** At Thermo Fisher Scientific , you will discover meaningful work that makes a positive impact on a ... North America. We are looking for a Senior Medical Writer to be dedicated to a client in the...the FSP team, you will provide high-quality medical and scientific writing from planning and coordination through delivery of… more
- Houston Methodist (Houston, TX)
- At Houston Methodist, the Senior Scientific Writer is responsible for functioning as the mentor for junior staff with an extensive knowledge of both medical and ... ESSENTIAL FUNCTIONS** + Prepares moderately complex documents and sections of regulatory submissions and contributes scientific knowledge and analytical skills… more
- University of Miami (Miami, FL)
- …. The Sylvester Comprehensive Cancer Center has an outstanding opportunity for a Scientific Writer 2 with experience in grant writing and manuscript preparation ... . The Scientific Writer analyzes, simplifies, writes, and designs...data from clinical studies for submission to governmental and regulatory agencies. + Edits all extramurally funded proposals for… more
- MD Anderson Cancer Center (Houston, TX)
- …patient education/materials, IRB forms. Works collaboratively with research nurse manager and regulatory staff to develop or coordinate the development of the study ... patient education/materials, IRB forms. Works collaboratively with research nurse manager and regulatory staff to develop or coordinate the development of the study… more
- IQVIA (Durham, NC)
- We are seeking a ** Scientific Writer - Vaccines** to join Q2 Solutions, IQVIA's laboratory business as a remote position. We hire passionate innovators who drive ... we transform and accelerate research and development. As a Scientific Writer - Vaccines, you will be...senior support, and staying updated on medical/technical writing and regulatory knowledge, including GCP and advances in drug development.… more
- McLaren Health Care (Detroit, MI)
- **Position Summary:** **The Scientific /Medical Writer ** plays a critical role in the development and execution of Karmanos Cancer Institute (KCI) oncology ... of a clinical trial. This role requires a combination of scientific knowledge, attention to detail, and excellent writing skills. **Responsibilities** **:**… more
- Capgemini (Richmond, VA)
- **Job description:** Capgemini Engineering is looking for a Technical Writer to work closely with Regulatory compliance team in an Agile environment for ensuring ... 100% regulatory compliance alignment) within the consumer products domain! **Key...tables. + Expert review of externally and internally generated scientific literature, appendices, data, reports, statistical models etc. +… more
- Abbott (Santa Clara, CA)
- …and interact with regulatory agencies' representatives as needed. The role of Scientific CER Writer /PM plays a significant part in new product development, ... fingersticks. **The Opportunity** The function of a **Senior Medical Writer /Project Manager** supporting our Structural Heart Clinical Evaluation Products combines… more
- Medical Mutual of Ohio (OH)
- …Cleveland, Ohio area residents preferred._** **Responsibilities** **Healthcare Analyst- Policy Writer ** + **Researches and analyzes evidence and background materials ... may include identification of specialty society positions, identification of regulatory findings specific to technologies, identification of coding specific… more
- MicroVention, Inc. (Tustin, CA)
- … scientific experience. 3. Demonstrated experience in the development of regulatory / clinical submissions (preferably as a medical writer for pharmaceutical, ... **12078BR** **Title:** Sr. Medical Writer **Job Description:** **INNOVATION STARTS WITH YOU** Are...job duties include: + Collaborating with the clinical & regulatory teams to write clinical documents for regulatory… more
- Reynolds American (Washington, DC)
- …Affairs **Number of Direct Reports** 0 **Core Relationships** Global Life Sciences, Scientific & Regulatory Affairs, Business Communications, Legal and External ... Medical Writer (Science & Public Health Affairs) Reynolds American...& PUBLIC HEALTH AFFAIRS)** **SENIORITY LEVEL:** Junior Level **FUNCTION:** Scientific Research & Development **LOCATION:** Washington DC **ROLE POSITIONING… more
- MicroVention, Inc. (Aliso Viejo, CA)
- **12251BR** **Title:** Sr. Medical Writer (PhD or MD) **Job Description:** **INNOVATION STARTS WITH YOU** Are you interested in working for an organization that is ... **TERUMO** has to offer. **Position Overview** The Sr. Medical Writer /Medical Writer will act as primary contact...job duties include: + Collaborating with the clinical & regulatory teams to write clinical documents for regulatory… more
- Charles River Laboratories (Charleston, SC)
- …Summary** **Charles River Labs based in Charleston, SC is seeking a Technical Writer 2 for our Research & Development Engineering team.** Technical writers plan, ... to the overall success of our products and services. As a Technical Writer for the Microbial Solutions Research and Development team, you will be collaborating… more
- Publicis Groupe (Philadelphia, PA)
- …inspire HCPs, and ultimately lead to improved patient outcomes. Given our scientific and medical talent, powerful data warehouse and creative digital solutions, we ... current clients are excited about a more modern medical communications and scientific exchange that delivers a future-forward customer experience and meets the… more
- DRT Strategies, Inc. (Silver Spring, MD)
- …will wow us even more if you have these skills: - Work experience as a scientific writer . - Experience with the FDA and/or pharmaceutical industry. - Savvy with ... track changes. - Ability to read, generate, and edit scientific content, such as journal articles or regulatory... scientific content, such as journal articles or regulatory documents - Ability to fact-check scientific … more
- IQVIA (Ithaca, NY)
- …in collaboration with senior staff. + Keep abreast of current data, trends, scientific writing/ regulatory knowledge, developments, and advances in area of drug ... We are seeking a **Medical Writer ** to join Q2 Solutions, IQVIA's laboratory business...development/ scientific writing. **What We Are Looking For:** + Bachelor's… more
