As a community, the University of Rochester is defined by a deep commitment to Meliora - Ever Better. Embedded in that ideal are the values we share: equity, leadership, integrity, openness, respect, and accountability. Together, we will set the highest standards for how we treat each other to ensure our community is welcoming to all and is a place where all can thrive.

MINIMUM EDUCATION & EXPERIENCE

• Bachelor’s degree in life sciences, health sciences, or related field Required
• Advanced degree (MS, MPH, PhD, PharmD) Preferred
• 3 years of experience in medical writing, preferably in clinical research, pharmaceutical, or academic setting or equivalent combination of education and experience Required
• Experience in a healthcare, academic medical center, or regulatory setting Preferred
• 3 years of experience in medical writing, preferably in clinical research, pharmaceutical, or academic setting or equivalent combination of education and experience RequiredExperience in a healthcare, academic medical center, or regulatory setting Preferred

KNOWLEDGE, SKILLS AND ABILITIES

• Excellent communication skills, with a strong command of English grammar and scientific terminology Required
• Proficiency in interpreting clinical trial data and writing in compliance with regulatory and scientific standards Required
• Familiarity with referencing tools (e.g., EndNote, Zotero) and document management systems Required
• Knowledge of relevant guidelines (e.g., ICH E3, CONSORT, GPP) and publication practices required Required
• Strong organizational and time management skills with the ability to manage multiple projects and deadlines simultaneously Required
  The University of Rochester is committed to fostering, cultivating, and preserving an inclusive and welcoming culture to advance the University’s Mission to Learn, Discover, Heal, Create – and Make the World Ever Better. In support of our values and those of our society, the University is committed to not discriminating on the basis of age, color, disability, ethnicity, gender identity or expression, genetic information, marital status, military/veteran status, national origin, race, religion, creed, sex, sexual orientation, citizenship status, or any other characteristic protected by federal, state, or local law (Protected Characteristics). This commitment extends to non-discrimination in the administration of our policies, admissions, employment, access, and recruitment of candidates, for all persons consistent with our values and based on applicable law.

GENERAL PURPOSE

The CHeT Communication Specialist II is responsible for the creation, development, and management of a wide range of scientific and medical documents in support of clinical, regulatory, and collaborative functions across CHeT. Ensures accuracy, clarity, and alignment of content with applicable guidelines and internal standards. Collaborates with internal and external stakeholders to produce high-quality materials for scientific and professional audiences. Manages timelines and deliverables across multiple projects and therapeutic areas, while maintaining compliance with medical writing standards and regulatory requirements.

ESSENTIAL FUNCTIONS

• Develops and authors a variety of scientific documents including clinical study reports (CSRs), investigator brochures, protocols, abstracts, manuscripts, regulatory submissions, slide decks, and other materials for internal and external dissemination.
• Collaborates with cross-functional teams and divisions throughout CHeT and the University of Rochester to ensure scientific accuracy, consistency, and adherence to timelines.
• Ensures all content complies with applicable guidelines such as ICH, GCP, and AMA Manual of Style, as well as University of Rochester policies, branding, and messaging standards.
• Synthesizes complex scientific and clinical data into clear, compelling narratives suitable for a range of audiences, including healthcare professionals, regulatory agencies, and the scientific community.
• Conducts thorough literature reviews and reference checks to support scientific content and provide up-to-date contextual framing of clinical data.
• Manages document timelines, project workflows, and version control to ensure deliverables are completed efficiently and accurately.
• Participates in strategic publication planning and contributes to the development and execution of publication plans across therapeutic areas.
• Provides input into processes and best practices for medical writing, including template development, style guides, and review procedures.
  Other duties as assigned.