Senior Medical Writer

Centessa Pharmaceuticals, a wholly subsidiary of Eli Lilly and Company, is advancing a portfolio of high‑conviction programs with strong biological validation. The company operates an asset‑centric model aimed at improving productivity while maintaining minimal centralized infrastructure. Description of Role The Senior Medical Writer will author and manage clinical regulatory documents in support of the company’s clinical development program, reporting to the Director of Medical Writing Operations. The role ensures high‑quality, consistent, and accurate deliverables across the development portfolio. Key Responsibilities Author and provide support for medical writing content, including study‑level documents such as clinical protocols, investigator brochures, clinical study reports, and other regulatory submissions. Collaborate closely with Clinical Development, Regulatory Affairs, Biostatistics, Pharmacovigilance, CMC, and Project Management teams. Partner with internal and external writers as necessary to support document completion. Oversee document preparation from start to finish—kick‑off, drafting, review cycles, feedback integration, quality control, and final delivery within timelines. Ensure clarity, consistency, and proper formatting of clinical documents across programs. Maintain compliance with GCP, ICH, eCTD, and company guidelines. Interpret complex clinical data and information. Demontrate strategic thinking and review capabilities. Contribute to the development and improvement of SOPs, templates, and document standards. Qualifications Advanced degree: PhD, PharmD, Master’s in a scientific/clinical field or English. 4+ years of medical writing or relevant pharmaceutical industry experience, including at least 2 years in sponsor‑level clinical/regulatory medical writing. Strong organizational, communication, and influencing skills; ability to prioritize, multitask, and deliver high‑quality documents under tight timelines. Flexibility and comfort with evolving priorities and targets. Understanding of drug development, biostatistics, and medical terminology; basic knowledge of scientific methodology as applied to drug development. Knowledge of global clinical trials and regulatory submission requirements (FDA, EMA, PMDA) and associated standards (ICH, GCP, CTD/eCTD, EU privacy regulations). Proficiency in Microsoft Word (advanced features) and familiarity with document management and collaborative authoring platforms (e.g., Veeva Vault, Please Review). Ability to work independently and collaboratively in a dynamic, fast‑paced, cross‑functional environment. Highly accurate, detail‑oriented, and professional with excellent interpersonal skills and a calm, diplomatic approach to challenges. Compensation The annual base salary range for this position is $150,000.00 to $180,000.00. Compensation will be determined based on qualifications, skills, relevant experience, and job knowledge. The role also offers a discretionary annual bonus and a comprehensive benefits package, including 401(k), medical, dental, vision, and life insurance, paid time off, and a wellness program. Work Location The Senior Medical Writer role is based in the United States, with occasional travel. Position Type Full‑Time, Exempt EEOC Statement Centessa Pharmaceuticals, a wholly owned subsidiary of Eli Lilly and Company, believes in a diverse environment and is committed to equal employment opportunity for all its employees and qualified applicants. We do not discriminate in recruitment, hiring, training, promotion, or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. We will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law. #J-18808-Ljbffr Centessa Pharmaceuticals, a wholly owned subsidiary of Eli Lilly and Company