Scientific Content Developer (Technical Writer III)

Scientific Content Developer (Technical Writer III)

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Job Description

We are seeking a talented and detail-oriented Scientific Content Developer to spearhead a critical R&D initiative. The successful candidate will be responsible for creating a internal playbooks a comprehensive guide that documents our cutting-edge scientific methodologies for advancing complex R&D programs. This role is essential for capturing and codifying institutional knowledge, ensuring that our innovative approaches can be scaled and applied consistently across our scientific teams to accelerate the delivery of new medicines to patients.

Responsibilities

Collaborate closely with subject matter experts across diverse R&D functions, including wet lab biology, computational biology, clinical development, and safety assessment.

Conduct structured interviews with our scientists and project teams to deeply understand and document their established processes and key decision-making frameworks.

Synthesize complex information from a variety of sources, including internal presentations, research documents, and scientific literature, into clear and accessible content.

Author well-structured, concise, and actionable content that serves as a practical guide for scientific teams.

Organize the playbook into a logical, user-friendly format that is easy for scientists to navigate and apply to their own projects.

Design and build the playbook as a dynamic, "living resource" on a digital platform such as SharePoint or Confluence to allow for easy updates and integration of supporting materials. (Preferred)

Manage project timeline effectively to ensure the timely delivery of content "chapters" and incorporate feedback from scientific reviewers.

Requirements

Bachelor's or advanced degree in a life science discipline.

5 years' experience in technical writing, medical writing, or a similar scientific communications role within the pharmaceutical or biotechnology industry.

Demonstrated ability to synthesize complex scientific concepts and processes into clear, well-structured documentation for a scientific audience.

Exceptional writing, editing, and proofreading skills with a keen eye for detail, consistency, and accuracy.

Broad understanding of the biopharma research and development process, from early discovery through clinical development.

Excellent interpersonal skills with the ability to interview subject matter experts, build rapport, and facilitate productive conversations.

Self-motivated and able to work independently, with good project management skills to manage competing priorities.

Demonstrated experience creating and managing content on a digital collaboration platform (e.g., SharePoint, Confluence, or similar wiki-based systems).

Familiarity with therapeutic development in immunology.

Seniority level

Mid-Senior level

Employment type

Full-time

Job function

Marketing, Public Relations, and Writing / Editing

Industries

Advertising Services and Civil Engineering

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