Clinical SOP Writer
PART/FULL TIME - 20-40 HOURS A WEEK

The Clinical SOP Writer works with Process Owners, Subject Matter Experts (SMEs), and relevant stakeholders to develop new and revise existing clinical procedures. The Writer ensures procedures and associated forms and templates are written to a high-quality standard and according to Eisai's writing style guide and to standards for clinical procedures/documents. The Clinical SOP Writer may also perform QC review of clinical procedures.

Requirements
* Bachelor's degree in English or related subject, or Bachelor's degree in science with proven writing experience
* Proven writing, editing, and quality control review experience. Proficiency in MS Word and Excel, experience in applying writing style guidelines and standards
* 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
* Customer-focused approach, with strong project management, multitasking, and interpersonal skills. Excellent communication skills both oral and written at all levels

Impellam Group and its brands are equal-opportunity employers committed to diversity and inclusion. All qualified applicants will receive consideration without regard to race, color, religion, gender, sexual orientation, pregnancy or maternity, national origin, age, disability, veteran status, or any other factor determined to be unlawful under applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application, interview process, pre-employment activity, and the performance of crucial job functions.

If you require additional disability considerations, modifications, or adjustments please let us know by contacting HR-InfoImpellamNA@impellam.com or fill out this form to request accommodations.