Location : Cambridge, MA (Hybrid) Science/ Focus: Cell Therapy Job Overview: This role is for a skilled Medical Writer to create and refine essential documents for clinical studies and regulatory submissions on a part-time basis. Primary Job Responsibilities: Lead and write clinical documents like protocols, reports, brochures, and regulatory submissions. Lead meetings for document development and review. Maintain writing timelines, standards, and processes for clinical and regulatory documents. Review statistical plans for data alignment in reports and summaries. Primary Job Requirements: Bachelors Degree and 5+ years in medical writing, ideally in cell therapy. Experienced in drug development, clinical study design, and documentation. Adept at writing and editing clinical protocols, reports, and INDs. Skilled in simplifying scientific content, with proficiency in Microsoft Office and foundational biostatistics and research knowledge. About Stratacuity: Whether you are seeking a career change or simply interested in becoming part of our network, you will appreciate the ethics guiding each Stratacuity team member. We build lasting relationships with exceptional biopharmaceutical talent and take great care to protect your personal information. Upon receiving your inquiry, you may be directly contacted by a Stratacuity team member to discuss your career goals. We will not share your information with anyone without your direct prior consent.
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