Associate Director, Medical Writing & Scientific Communications
$170,000–$190,000 year
On-siteSan Diego, California, United States
Job Summary
Develop and execute strategic medical writing and scientific communication plans aligned with Medical Affairs objectives. Lead the creation of high-quality deliverables including peer-reviewed manuscripts, abstracts, posters, oral presentations, and medical education resources. Partner with cross-functional stakeholders to establish scientific narratives and disease-state education platforms while ensuring communications are accurate, compliant, and aligned with GPP and ICMJE guidelines. Translate complex clinical trial data into clear communications for healthcare professionals and investigators. Manage external medical writing agencies and establish scalable writing processes and best practices. Support Medical Science Liaison training, investigator meetings, and congress planning. Maintain scientific expertise through ongoing review of clinical data and competitive intelligence. Collaborate closely with Clinical Development, Regulatory Affairs, and Commercial teams to ensure consistent scientific messaging.
Required Qualifications
- Minimum of 5 years of progressive experience in medical writing, scientific communications, medical affairs, or related roles within a biotechnology or pharmaceutical organization
- Demonstrated experience developing peer-reviewed publications, scientific congress materials, and clinical communication deliverables
- Current experience supporting Medical Affairs, Scientific Affairs, Clinical Development, or related functions within a biotechnology or pharmaceutical industry
- Strong understanding of clinical trial design, interpretation of clinical data, and evidence-based scientific communication
- Exceptional scientific writing, editing, and communication skills with strong attention to detail
- Ability to synthesize complex scientific information and communicate actionable insights to diverse audiences
- Experience developing strategic scientific narratives and communication platforms
- Strong knowledge of publication standards, including GPP and ICMJE guidelines
- Ability to manage multiple projects, priorities, and timelines in a fast-paced environment
- Strong analytical, organizational, and problem-solving skills
- Demonstrated ability to collaborate effectively with internal and external partners
- Self-motivated individual with an entrepreneurial mindset and ability to operate independently
- Strong interpersonal skills and professional demeanor
- Excellent verbal and written communication skills
- Proficiency with Microsoft Office Suite (Word, PowerPoint, Excel), collaboration platforms, and virtual communication tools
Desired Qualifications
- Pharm.D., Ph.D., M.D., D.O., or other advanced scientific degree preferred
- Proven scientific expertise in obesity, cardiometabolic disease, metabolic disorders, or related therapeutic areas preferred
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