Senior Medical Writer

4+ years of medical writing or relevant pharmaceutical industry experience, including at least 2 years in sponsor-level clinical/regulatory medical writing.

Previous neuroscience experience is strongly preferred.

Understanding of drug development, biostatistics, and medical terminology; basic understanding of scientific methodology as applied to drug development.

Knowledge of global clinical trials and regulatory submission requirements (FDA, EMA, PMDA), including ICH, GCP, CTD/eCTD, and EU privacy/redaction regulations.

The annual base salary range for this position is $150,000.00 to $180,000.00. Individual compensation within this range will be determined based on a variety of factors, including qualifications, skills, relevant experience, and job knowledge.

In addition to base pay, this role is eligible for a discretionary annual bonus. Centessa also offers a comprehensive benefits package, which includes a 401(k) plan, company-sponsored medical, dental, vision, and life insurance, generous paid time off, and a health and wellness program.

Author and provide support for medical writing content, including but not limited to study level documents (clinical protocols and amendments, Investigator Brochures, clinical study reports), agency requests for information, IND/CTA submission documents, NDA/MAA clinical modules and summary documents, and other writing as necessary.

Collaborate closely with relevant functions, including Clinical Development, Regulatory Affairs, Biostatistics, Pharmacovigilance, CMC, and Project Management teams.

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.

Contribute to the development and improvement of SOPs, templates, and document standards.