Scientific Writer
Radiant Systems Inc, Newark, DE, United States
Client: Major Agriscience Client
Position: Scientific Writer
Duration: 12 Months Contract
Location: Newark DE 19711
Pay Rate: $30.00-$34.00/ Hr on W2
Description This is a Scientific Writer contractor position supporting Global Regulatory Science Operations.
The Scientific Writer will be responsible for drafting and finalizing toxicology protocols, study reports, and study summaries to support regulatory submissions.
The role requires strong scientific writing skills, a solid understanding of Good Laboratory Practice (GLP), and the ability to collaborate effectively with cross-functional stakeholders.
Preferred Skills & Experience
Bachelor’s degree in Biology, Microbiology, or a related scientific discipline
Prior experience with scientific writing and GLP preferred
Ability to manage multiple projects simultaneously and meet tight deadlines
Strong attention to detail
Experience using Adobe Acrobat Pro to compile and edit documents preferred
Proficient in Microsoft Office Suite and document management systems
Job Summary
Draft high-quality toxicology protocols, study reports, and study summaries to support regulatory submissions
Utilize strong scientific writing skills with a background in toxicology or related biological sciences
Perform quality control (QC) reviews on draft reports with an understanding of Good Laboratory Practice (GLP)
Contribute to the development and revision of report templates and assist with process optimization effortsFacilitate finalization of reports and audit responsesCommunicate effectively with key stakeholders
Partner with stakeholders to understand regulatory reporting requirements
Job Requirements
Bachelor’s degree or higher in Biology, Microbiology, or a related scientific discipline
Demonstrated experience in scientific writing, preferably within a regulatory environment
Strong understanding of Good Laboratory Practice (GLP) standards and regulatory guidelines
Excellent attention to detail with the ability to perform quality control reviews
Proficiency in Microsoft Office Suite and document management systems
Strong communication and collaboration skills
Ability to manage multiple projects and meet tight deadlines
Experience using Adobe Acrobat Pro is preferred
#J-18808-Ljbffr
Position: Scientific Writer
Duration: 12 Months Contract
Location: Newark DE 19711
Pay Rate: $30.00-$34.00/ Hr on W2
Description This is a Scientific Writer contractor position supporting Global Regulatory Science Operations.
The Scientific Writer will be responsible for drafting and finalizing toxicology protocols, study reports, and study summaries to support regulatory submissions.
The role requires strong scientific writing skills, a solid understanding of Good Laboratory Practice (GLP), and the ability to collaborate effectively with cross-functional stakeholders.
Preferred Skills & Experience
Bachelor’s degree in Biology, Microbiology, or a related scientific discipline
Prior experience with scientific writing and GLP preferred
Ability to manage multiple projects simultaneously and meet tight deadlines
Strong attention to detail
Experience using Adobe Acrobat Pro to compile and edit documents preferred
Proficient in Microsoft Office Suite and document management systems
Job Summary
Draft high-quality toxicology protocols, study reports, and study summaries to support regulatory submissions
Utilize strong scientific writing skills with a background in toxicology or related biological sciences
Perform quality control (QC) reviews on draft reports with an understanding of Good Laboratory Practice (GLP)
Contribute to the development and revision of report templates and assist with process optimization effortsFacilitate finalization of reports and audit responsesCommunicate effectively with key stakeholders
Partner with stakeholders to understand regulatory reporting requirements
Job Requirements
Bachelor’s degree or higher in Biology, Microbiology, or a related scientific discipline
Demonstrated experience in scientific writing, preferably within a regulatory environment
Strong understanding of Good Laboratory Practice (GLP) standards and regulatory guidelines
Excellent attention to detail with the ability to perform quality control reviews
Proficiency in Microsoft Office Suite and document management systems
Strong communication and collaboration skills
Ability to manage multiple projects and meet tight deadlines
Experience using Adobe Acrobat Pro is preferred
#J-18808-Ljbffr