- ThermoFisher Scientific (Greenville, NC)
- **Work Schedule** Standard (Mon-Fri) **Environmental Conditions** Office **Job Description** ** Principal Medical Writer ** At Thermo Fisher Scientific, you'll ... team is growing, and we are looking for a Principal Medical Writer . This role...research. Your expertise will enable us to deliver flawless Regulatory Medical Writing documents, such as protocols,… more
- ThermoFisher Scientific (Greenville, NC)
- …Schedule** Standard (Mon-Fri) **Environmental Conditions** Office **Job Description** **FSP Senior** ** Regulatory ** ** Medical Writer (** **Remote;** **US** ... candidates based in the US! As a remote-based Senior Medical Writer within the FSP team, you...possess the versatility to author both clinical and preclinical regulatory documents, with therapeutic area expertise in infectious diseases… more
- Parexel (Jefferson City, MO)
- **Job Summary:** The Senior Medical Writer will research, create, and edit all documents associated with clinical research. Responsibilities also include: acting ... by Medical Writing Support Coordinator, Document Specialist, and/or Associate Medical Writer for assembly of project files and client deliverables.… more
- Stony Brook University (Stony Brook, NY)
- Stony Brook Cancer Center Grant and Protocol Development Writer **Required Qualifications:** (as evidenced by an attached resume) * Ph.D., MD, or equivalent advanced ... writing, research development, or protocol writing within an academic medical or research setting. * Experience drafting or coordinating investigator-initiated… more
- University of Miami (Miami, FL)
- …Miami/UHealth Department of SCCC has an exciting opportunity for a Full Time Hybrid Scientific Writer 2 to work at the UHealth medical campus in Miami, Fl. CORE ... SUMMARYThe Hybrid (1X a week or as necessary) Scientific Writer 2 collects and analyzes complex scientific data and...of the target audience. This job also assists the Principal Investigator (PI) with the development and/or completion of… more
- AbbVie (North Chicago, IL)
- …thorough theoretical and practical understanding of own scientific discipline. + Effective writer and communicator of research or other regulatory materials. ... that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a...Job Description Purpose: AbbVie is looking for a Sr. Principal Systems Engineer to join their Combination Product Development… more
- IQVIA (Durham, NC)
- …teams that include Project Manager, CRA, Data Manager, Biostatistician, Programmer, and/or Medical Writer . + Maintain awareness of overall developments in the ... **Job Level:** Senior/ Principal Pharmacometrician, FSP **Location:** Home-based in the US...sections of dossiers for product registration and communicate with regulatory agencies. + Assess pharmacometric requirements for and ensure… more
- Microsoft Corporation (Redmond, WA)
- …critical priorities for our customers in a world awash in digital threats, regulatory scrutiny, and estate complexity. Microsoft Security aspires to make the world a ... be an opportunity for you. The security team seeks a motivated, experienced Principal Technical Security Program Manager to join our benchmarking team. We are… more
- Republic Services (Elizabeth, NJ)
- …a direct extension to the sales and customer service teams. ** PRINCIPAL RESPONSIBILITIES:** + Collaborate with cross-functional teams to troubleshoot technical ... sales department to offer solutions that meet quality and regulatory standards, performs technical evaluations, facilitates communication between departments,… more