Strategic Medical Writing & Scientific Communications Lead

Viking Therapeutics

San Diego (CA)

On-site

USD 170,000 - 190,000

Full time

14 days+

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Job summary

Viking Therapeutics, Inc. is seeking an Associate Director, Medical Writing & Scientific Communications to shape strategic medical communications across publications, congress activities, and advisory boards.

You will lead high-quality manuscripts, abstracts, posters, and educational resources to support clinical development and launch readiness. The ideal candidate has a strong track record in medical writing within biotechnology/pharma, cross-functional collaboration, and the ability to

Qualifications

  • Pharm.D., Ph.D., M.D., D.O., or other advanced scientific degree preferred.
  • 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 the biotechnology or pharmaceutical industry.
  • Proven scientific expertise in obesity, cardiometabolic disease, metabolic disorders, or related therapeutic areas preferred.
  • Strong understanding of clinical trial design, interpretation of clinical data, and evidence-based scientific communication.

Responsibilities

  • Develop and execute strategic medical writing and scientific communication plans aligned with Medical Affairs objectives and company priorities.
  • Lead the development of scientific communication deliverables, including peer-reviewed manuscripts, abstracts, posters, oral presentations, scientific slide decks, advisory board materials, and medical education resources.
  • Partner with Medical Affairs leadership and cross-functional stakeholders to establish scientific narratives, evidence communication strategies, and disease-state education platforms.
  • Support publication planning activities, including development and execution of publication plans in collaboration with internal stakeholders, external authors, and medical writing agencies.
  • Ensure scientific communications are accurate, balanced, compliant, and aligned with applicable guidelines, including GPP and ICMJE recommendations.
  • Translate complex clinical trial data, scientific literature, and healthcare trends into clear and compelling communications for healthcare professionals, investigators, and internal stakeholders.
  • Support medical affairs activities including: Medical Science Liaison training and scientific preparation; Investigator meetings; Advisory boards; Congress planning and execution; Medical information resources; Internal scientific communications.
  • Collaborate closely with Clinical Development, Regulatory Affairs, Biostatistics, Commercial, Market Access, and other internal partners to ensure consistency of scientific messaging.
  • Manage external medical writing agencies, consultants, and scientific communication vendors.
  • Establish scalable medical writing processes, templates, and best practices to support a growing Medical Affairs organization.
  • Lead and/or contribute to cross-functional project teams supporting scientific communications strategy and execution.
  • Maintain and continuously enhance scientific expertise through ongoing review of clinical data, scientific literature, healthcare trends, and competitive intelligence.

Skills

Scientific writing
Medical communications
Publication planning
Cross-functional collaboration

Education

Advanced scientific degree

Tools

MS Office

Job description

Viking Therapeutics, Inc. is seeking an Associate Director, Medical Writing & Scientific Communications to shape strategic medical communications across publications, congress activities, and advisory boards.

You will lead high-quality manuscripts, abstracts, posters, and educational resources to support clinical development and launch readiness. The ideal candidate has a strong track record in medical writing within biotechnology/pharma, cross-functional collaboration, and the ability to

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