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CDI Specialist: Clinical Documentation Excellence (Remote) in Minot
Trinity Health in the United States is seeking a CDI Specialist to improve the accuracy, clarity, and completeness of clinical documentation across inpatient, same-day surgery, observation, and emergency encounters.
You will perform concurrent medical record reviews, identify opportunities ...Read more
Inpatient CDI Specialist: Documentation & Utilization in Shelbyville
Major Hospital is seeking a Clinical Documentation Specialist to review and analyze medical records, identifying relevant diagnoses and procedures for distinct patient encounters. The role requires staying current with federal and state regulations impacting prospective payment and clinical treat ...Read more
CMC Technical Writer - Synthetic Chemistry in Boston
Company Description
The work we do at Eurofins Professional Scientific Services matters, and so do our employees. At Eurofins PSS, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bott ...Read more
CMC Technical Writer: Late-Stage Lipids & Process Chemistry (Hybrid) in Boston
Eurofins USA PSS Insourcing Solutions is seeking a CMC Technical Writer to support Late-Stage Lipids process chemistry and regulatory documentation. You will translate complex data into clear narratives and ensure traceable, inspection-ready records.
The role emphasizes collaboration with C ...Read more
Remote CMC Technical Writer — Regulatory & Analytical Expert in Boston
Centessa Pharmaceuticals seeks a Contract CMC Technical Writer to critically review data, methods, batch records, and development reports from external CDMOs to finalize source documents for analytical, drug substance and drug product, and to prepare regulatory content and summaries.
You wi ...Read more
Remote CMC Technical Writer – Contract in Boston
Centessa Pharmaceuticals, a wholly owned subsidiary of Eli Lilly and Company, is seeking a Contract CMC Technical Writer to critically review data, batch records, and development reports from external CDMOs to finalize source documents for analytical, drug substance and drug product.
The ro ...Read more