
Scientific Writer
SPECTRAFORCE, Newark, DE, United States
Job Title: Regulatory Specialist
Location: Newark, DE 19711
Duration: 12 Months (Possibility of extension depending upon business requirements and performance)
Shift: 8am-5pm
Pay Range: $30.00 - $34.28/hour
Description:
Regulatory Specialist-Scientific Writer
- This is a Scientific Writer contractor position supporting Global Regulatory Science Operations at the Haskell Research Station.
- The Scientific Writer will be responsible for drafting and finalizing toxicology protocols, study reports, and study summaries to support regulatory submissions for crop protection products.
- 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.
Additional:
- Any specific skills, requirements or experience you want in a candidate: BS in biology, microbiology, or a related scientific discipline.
- Prior experience with scientific writing and GLP experience 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 is preferred.
- Proficient in using Microsoft Office Suite and document management systems.
- Any additional Medical Surveillance testing required? No
- Any exposure to common allergens? No
- Will non-local/remote candidates be considered? No
Job Summary:
- Draft high-quality toxicology protocols, study reports and study summaries to support Crop Protection regulatory submissions.
- Strong scientific writing skills and a background in mammalian toxicology, ecotoxicology, or related biological science are needed for drafting reports.
- Perform quality control (QC) reviews on draft reports. An understanding of Good Laboratory Practice (GLP) is required.
- Contribute to the development and revision of report templates and assist with process optimization efforts.
- Facilitate finalization of reports and audit responses.
- Communicate effectively with key stakeholders and customers.
- Partner with stakeholders and customers 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 the regulatory or crop protection industry.
- Strong understanding of Good Laboratory Practice (GLP) standards and regulatory guidelines.
- Excellent attention to detail and ability to perform quality control reviews on scientific documents.
- Proficient in using Microsoft Office Suite and document management systems.
- Effective communication and collaboration skills with cross-functional teams and stakeholders.
- Ability to manage multiple projects simultaneously and meet tight deadlines.
- Experience using Adobe Acrobat Pro to compile and edit documents is preferred.