Biotech and Pharmaceutical, Communication Skills, Customer Relations, Drug Development, Editing, English Language, GCP (Good Clinical Practices), ICH Regulations, Interpersonal Skills, Medical Writing, Microsoft Excel, Microsoft Word, Multitasking, Presentation/Verbal Skills, Project/Program Management, Quality Control, Regulatory Compliance, Regulatory Requirements, Standard Operating Procedures (SOP), Style Guide, Writing Skills
Title: SOP Writer Location: Nutley, NJ- Hybrid Duration: 12 Months+ Possible Extension Pay Range: $42- $47/hr Requirements Bachelors degree in English or related subject, or Bachelors degree in science with proven writing experience. Experience of working with multiple disciplines in clinical development in the pharmaceutical industry, with knowledge of the drug development process. A working knowledge of compliance standards, and ICH, GCP, and regulatory requirements. Proven writing, editing, and quality control review experience. Proficiency in MS Word and Excel, experience in applying writing style guidelines and standards. Customer-focused approach, with strong project management, multitasking, and interpersonal skills. Excellent communication skills both oral and written at all levels. 3-5 years pharma/biotech experiences. Previous medical writing experiences preferred.I
Integrated Resources, Inc