Ardelyx is looking for a Medical Writer to join our team. You will develop high-quality clinical documentation in compliance with regulatory standards, playing a critical role in our medical information strategies and business objectives. This position offers the opportunity to work in a collaborative, dynamic environment.

What You'll Do

Develop high-quality clinical documents ensuring scientific excellence and regulatory compliance.
Write, format, and edit clear, concise content for various materials, adhering to style guidelines.
Ensure compliance of clinical documents with regulatory requirements.
Provide scientific evaluation of company products to key internal stakeholders.
Collaborate with cross-functional teams to implement medical-driven communication strategies.
Act as a scientific point of contact within the company.
Prepare document timelines, with guidance from manager, as needed.
Conduct literature searches and summarize data from statistical tables as needed.
Coordinate quality control reviews of clinical documents and maintain audit trails.
Develop clear, accurate, and visually engaging graphic content, including tables and figures.
Design and develop scientific posters for congresses.
Review and ensure the accuracy, clarity, and consistency of all clinical documents.

What We're Looking For

Master’s degree with 3+ years of medical writing experience in the pharmaceutical or biotechnology industry.
Strong understanding of regulatory submission requirements.
Exceptional writing, editing, and formatting skills.
Detail-oriented with a focus on accuracy and precision.
Ability to interpret and summarize complex scientific data.
Excellent communication and interpersonal skills.
Proven ability to manage multiple projects and meet deadlines.
Strong organizational and project management skills.
Proficiency in graphic design software (Adobe, Microsoft Visio, GraphPad Prism, etc.).
Ability to work independently and as part of a team.