Culmen International is hiring a.Research Directorate at the Naval Air Warfare Center Aircraft Division and will be on-site in Lakehurst, NJ.The Naval Air Warfare Center Aircraft Division (NAWCAD) Lak...

As a Regulatory Affairs Specialist, you will play a pivotal role in monitoring regulatory developments, ensuring compliance, and driving regulatory excellence across multiple product categories, inclu...

Researching and consolidating regulatory requirements to enable future development of regulatory strategies for all regions. Respond to questions from regulatory agencies during review/submissions. Su...

The Regulatory Affairs Medical Writer supports regulatory submissions and clinical documentation by generating and maintaining regulatory deliverables that incorporate clinical data, scientific litera...

The Regulatory Affairs Medical Writer supports regulatory submissions and clinical documentation by generating and maintaining regulatory deliverables that incorporate clinical data, scientific litera...

The Medical Writer will primarily work on the development and delivery of high-quality documents such as Clinical protocols, protocol amendments, Investigator's Brochures (IBs), non-clinical and clini...

Initial draft authoring of scientific content for Common Technical Document (CTD) Quality sections and responses to health authority questions aligned with regulatory strategy for cell therapy clinica...

TEKsystems is hiring an Instructional Designer/Technical writer to join one of our non-profit insurance clients in NYC.

The Regulatory Affairs Medical Writer supports regulatory submissions and clinical documentation by generating and maintaining regulatory deliverables that incorporate clinical data, scientific litera...

The Regulatory Affairs Medical Writer supports regulatory submissions and clinical documentation by generating and maintaining regulatory deliverables that incorporate clinical data, scientific litera...

The Regulatory Affairs Medical Writer supports regulatory submissions and clinical documentation by generating and maintaining regulatory deliverables that incorporate clinical data, scientific litera...

The Regulatory Affairs Medical Writer supports regulatory submissions and clinical documentation by generating and maintaining regulatory deliverables that incorporate clinical data, scientific litera...

The Regulatory Affairs Medical Writer supports regulatory submissions and clinical documentation by generating and maintaining regulatory deliverables that incorporate clinical data, scientific litera...

The Regulatory Affairs Medical Writer supports regulatory submissions and clinical documentation by generating and maintaining regulatory deliverables that incorporate clinical data, scientific litera...

Location: Hybrid – Brooklyn, NY.Develop technical and functional documentation.Work with cross-functional teams to gather, translate, and document requirements.

The Regulatory Affairs Medical Writer supports regulatory submissions and clinical documentation by generating and maintaining regulatory deliverables that incorporate clinical data, scientific litera...

The Regulatory Affairs Medical Writer supports regulatory submissions and clinical documentation by generating and maintaining regulatory deliverables that incorporate clinical data, scientific litera...

The Regulatory Affairs Medical Writer supports regulatory submissions and clinical documentation by generating and maintaining regulatory deliverables that incorporate clinical data, scientific litera...

The Regulatory Affairs Medical Writer supports regulatory submissions and clinical documentation by generating and maintaining regulatory deliverables that incorporate clinical data, scientific litera...

Duration: 36 Months, extension possible based on needs and performance.Communicate and collaborate with various stakeholders to capture information, define business needs and document functional and t...

The Regulatory Affairs Medical Writer supports regulatory submissions and clinical documentation by generating and maintaining regulatory deliverables that incorporate clinical data, scientific litera...

The Regulatory Affairs Medical Writer supports regulatory submissions and clinical documentation by generating and maintaining regulatory deliverables that incorporate clinical data, scientific litera...

Location: Pittsburgh, PA/ NYC, NY (Weekly 3 Days onsite).Strong skills in technical writing tools (e.MS Word, Confluence, MadCap Flare, GitBook).Proficiency in video editing software (e.Adobe Premiere...

The Analytics Technical Writer will partner with multiple customers across the Enterprise to provide more complex resolutions to analytics/data problems (with a focus on Data Quality) which require a ...

Certifications: RAC (Regulatory Affairs Certification) or similar credentials are a plus. The Senior Regulatory Specialist must be experienced and thoughtful about the processes necessary for achievin...

Certifications: RAC (Regulatory Affairs Certification) or similar credentials are a plus. The Senior Regulatory Specialist must be experienced and thoughtful about the processes necessary for achievin...

The Senior Regulatory Affairs Specialist is responsible for planning and executing regulatory submissions and ensuring regulatory compliance. The individual combines knowledge of scientific, regulator...

The Senior Regulatory Affairs Specialist is responsible for planning and executing regulatory submissions and ensuring regulatory compliance. The individual combines knowledge of scientific, regulator...

Biostatistics, Data Management, Regulatory Affairs, Medical Affairs, Clinical Development, Clinical Operations and R&D Management to obtain necessary information and to ensure the timely implementatio...

Biostatistics, Data Management, Regulatory Affairs, Medical Affairs, Clinical Development, Clinical Operations and R&D Management to obtain necessary information and to ensure the timely implementatio...

Technical Writer needs technical Writing, Communications, or Medical Technology with technical writing experience. About the job Technical Writer.

Support internal and external Regulatory agency audits, providing Regulatory input to minimize potential findings of non-compliance. Stay abreast of Regulatory procedures and changes in the Regulatory...

Technology Regulatory Affairs Specialist.

Technology Regulatory Affairs Specialist.

As a Medical Writer II at ICON, you will play a pivotal role in the development and preparation of clinical trial documents, regulatory submissions, and scientific publications, contributing to the ad...

As a Medical Writer II at ICON, you will play a pivotal role in the development and preparation of clinical trial documents, regulatory submissions, and scientific publications, contributing to the ad...

We’re looking for a detail-oriented and process-focused Entry-Level Batch Record Reviewer to join our pharmaceutical manufacturing team.This role is ideal for someone with strong organizational skills...

Quality and Regulatory Affairs Specialist. Participates in the preparation, planning, coordination and oversight of planned and unplanned regulatory survey and reporting by The Joint Commission, New Y...

Tuesday/Wednesday/Thursday: 7:00 p.The Proofreader is responsible for proofreading and editing a variety of legal documents and other printed documentation, correcting format and style as well as corr...

Tuesday/Wednesday/Thursday: 7:00 p.The Proofreader is responsible for proofreading and editing a variety of legal documents and other printed documentation, correcting format and style as well as corr...