Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Associate Director, Medical Writing

Jazz Pharmaceuticals
Jazz Pharmaceuticals
5-8 years
$154,400 – $231,600
10 Dec. 22, 2025
Job Description
Job Type: Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Associate Director, Medical Writing – Global (Remote / Multiple Locations)

Company: Jazz Pharmaceuticals
Locations: Mississauga, ON, Canada | Cambridge, UK | London, UK | Carlsbad, CA | Palo Alto, CA | Philadelphia, PA – Remote/Home-Based Options Available
Category: Research & Development
Experience Required: 8+ years (BA/BS) or 5+ years (Advanced Degree) in pharmaceutical medical writing
Job ID: R010768


About Jazz Pharmaceuticals

Jazz Pharmaceuticals is a global biopharma leader dedicated to transforming patient lives through innovation. Our mission is to develop life-changing medicines for patients with serious diseases, often addressing conditions with limited or no therapeutic options.

With a robust pipeline in oncology, neuroscience, and rare diseases, Jazz combines scientific rigor with patient-focused innovation. Headquartered in Dublin, Ireland, Jazz operates research and development laboratories, manufacturing facilities, and offices worldwide, delivering solutions to patients globally. Learn more at www.jazzpharmaceuticals.com.


Role Overview

The Associate Director, Medical Writing will lead the preparation of high-quality medical writing deliverables across one or more global clinical programs. This includes regulatory documents such as protocols, clinical study reports (CSRs), briefing books, submission documents, and investigator brochures.

You will collaborate closely with cross-functional teams, ensuring strategic alignment of medical messaging, consistent data presentation, and adherence to global regulatory standards. This role may also involve management of medical writing teams and oversight of contract writers, with a focus on quality, compliance, and efficiency.


Key Responsibilities

  • Collaborate with cross-functional teams to ensure accurate and consistent medical communication across programs.

  • Author and review regulatory and clinical documents, ensuring alignment with program strategy and regulatory requirements.

  • Ensure quality control, accuracy, and compliance of all medical writing deliverables.

  • Manage and mentor internal and external writers, ensuring efficient delivery of program documentation.

  • Contribute to Best Practices and SOP development for medical writing processes.

  • Participate in global teams and interactions with regulatory agencies across regions.

  • Analyze complex clinical data and synthesize information for regulatory submission and communication purposes.


Qualifications & Skills

  • Education: BA/BS with 8+ years of pharmaceutical medical writing experience, or advanced degree (PharmD, PhD, MD, MSc) with 5+ years of experience.

  • Exceptional English writing and editing skills, with ability to convey complex scientific concepts clearly.

  • In-depth knowledge of ICH, CTD, and GCP guidelines.

  • Experience in lean authoring for clinical regulatory documents and global submissions.

  • Strong understanding of clinical development processes and submission requirements at all stages.

  • Proven ability to lead and manage complex medical writing projects.

  • Excellent project management, organizational, and time management skills.

  • Ability to collaborate in multicultural teams, build relationships, and influence stakeholders.

  • Knowledge of medical publication standards (ICMJE, AMA, GPP) preferred.

  • Proficient in MS Office suite, including Word, Excel, PowerPoint, and document formatting tools.


Why Join Jazz Pharmaceuticals?

  • Opportunity to work on high-impact global clinical programs across therapeutic areas.

  • Remote-friendly position with international collaboration opportunities.

  • Lead and mentor talented medical writing teams across global locations.

  • Competitive total compensation package, including base salary, annual bonus, and equity opportunities.

  • Comprehensive benefits: medical, dental, vision, retirement, and flexible PTO.

U.S. Salary Range: $154,400 – $231,600 (based on experience, skills, and location)


Equal Opportunity Employer

Jazz Pharmaceuticals is committed to equal opportunity employment and considers all qualified applicants without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or other legally protected characteristics.


Apply Now

Shape the future of global medical communications at Jazz Pharmaceuticals. Bring your expertise in medical writing and clinical documentation to an organization committed to innovative therapies and patient impact.

SEO Keywords Optimized: Medical Writing Jobs, Associate Director Medical Writing, Global Regulatory Writing, Clinical Study Reports, Pharmaceutical Writing Careers, Remote Medical Writing Jobs, Jazz Pharmaceuticals Careers, Medical Writing Leadership