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New · posted Oct 31

Iambic Therapeutics · Biotechnology

Principal Medical Writer

  • Remote, US
  • Remote
  • Full-time
  • Senior & Principal
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EmploymentFull-time
LocationRemote, US
DeadlineOpen until filled

The role

Iambic Therapeutics is seeking an experienced Principal Medical Writer to independently author and oversee development of high-quality submission-ready documents to support clinical-stage programs and IND submissions.

Reporting to the Head of Medical Writing, this role will partner with cross-functional stakeholders to advance Iambic’s mission of delivering highly differentiated, patient-optimized therapeutics to address urgent unmet medical needs. The ideal candidate will have strong scientific judgment, regulatory writing expertise, and the ability to thrive in a fast-moving, evolving organization.

What you need

  • Bachelor’s degree in a life science (or health-related field) required; advanced degree (Masters/PhD/PharmD) preferred with a minimum 10 years of relevant medical writing experience

  • Demonstrated experience with IND submissions and documents to support clinical-stage programs

  • Detail-oriented with excellent scientific writing, communication, and organizational skills

  • Highly skilled in Microsoft Office suite, particularly MS Word. Experience with electronic document and reference management systems preferred, with a demonstrated aptitude and interest in learning and adopting new technologies, including AI-enabled tools

  • Strong understanding of FDA/EMA regulations and ICH guidelines

  • Comfortable working and collaborating in a fast-paced environment

What you'll do

  • Responsible for planning, authoring, and delivery of submission-ready documents (protocols, IBs, DSURs, CSRs, INDs, Health Authority responses, and briefing documents etc.)

  • Independently lead cross-departmental document development by collaborating with the Clinical, Nonclinical, Medical, Biostatistics, CMC, and Regulatory teams

  • Represent medical writing on internal cross functional study teams and ad hoc working groups

  • Support development of abstracts, posters, and presentations for scientific conferences

  • Help establish and refine medical writing processes, templates, and standards to ensure consistency, quality, and accuracy across all deliverables. Implement and manage efficient document workflows and timelines

  • Participate in the evaluation and integration of AI-enabled tools to improve writing quality and efficiency

Pay and benefits

$152,000 – $190,000 a year

Employer provided
How this compares
  • Company-paid healthcare

  • Flexible spending accounts

  • Voluntary life insurance

  • 401(k) matching

  • Uncapped vacation

  • Onsite gym and dining

Two Iambic scientists in Iambic lab coats and safety glasses working with sample tubes at a lab bench

From the posting

About Iambic

ABOUT IAMBIC THERAPEUTICS

Iambic is a clinical-stage life-science and technology company developing novel medicines using its AI-driven discovery and development platform. Based in San Diego and founded in 2020, Iambic has assembled a world-class team that unites pioneering AI experts and experienced drug hunters. The Iambic platform has demonstrated delivery of new drug candidates to human clinical trials with unprecedented speed and across multiple target classes and mechanisms of action. Iambic is advancing a pipeline of potential best-in-class and first-in-class clinical assets, both internally and in partnership, to address urgent unmet patient need. Learn more about the Iambic team, platform, pipeline, and partnerships at iambic.ai.

MISSION & CORE VALUES

Our mission is to deliver better medicines through innovations in AI-based discovery technologies. The culture and work at Iambic Therapeutics are profoundly strengthened by the diversity of our people and our differences in background, culture, national origin, religion, sexual orientation, and life experiences. We are committed to building an inclusive environment where a diverse group of talented humans work together to discover therapeutics and create technologies.

PAY AND BENEFITS

We offer industry leading competitive pay, company paid healthcare, flexible spending accounts, voluntary life insurance, 401K matching, and uncapped vacation to our team. We are in a brand-new state-of-the art facility in beautiful San Diego with an onsite gym, dining, and easy access to great places to live and play.

Iambic company page · 7 open roles

Job intelligence

The context around this role

Live data · October 31, 2026

Salary intelligence

How the pay compares

This role's midpoint is 8% below the US median for Clinical Evaluation & Medical Writing roles at this level.

This roleEmployer provided

$152,000 to $190,000 a year

Senior & Principal roles in the US6 roles publishing pay

Middle half $162,375 to $205,875, median $186,000
Annual base pay
Annual base payLowMedianHigh
This role$152,000—$190,000
All US$162,375$186,000$205,875

This role: Iambic Therapeutics's own published range. Comparisons: the base pay employers published on open Clinical Evaluation & Medical Writing roles at the same level on Regulatory Jobs, October 31, 2026. Nothing is estimated.

Career trajectory

Where this role sits in Clinical Evaluation & Medical Writing

The general path across 21 open Clinical Evaluation & Medical Writing roles on Regulatory Jobs, with the titles they carry most. Not Iambic's own promotion track.

  1. One step back

    Associate & Specialist

    Often: Clinical Scientist Intern

  2. This role

    Senior & Principal

    Often: Principal Medical Writer · Senior Medical Writer

    $186K median8 open
  3. Next step

    Manager

    Often: Medical Writing Manager · Medical Writing Science Senior Manager

  4. Later

    Director

    Often: Director, Medical Writing · Associate Director, Medical Writing

    $207K median9 open

Skills DNA

What this role leans on

How many of the posting's 14 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.

GMP and compliance: 1 lineDocumentation and SOPs: 11 linesRegulatory submissions: 3 linesData and digital systems: 1 lineClinical trial conduct: 1 lineCollaboration and leadership: 5 linesGMPDocumentationSubmissionsData systemsClinical trialsTeamwork
  • Documentation and SOPs11
  • Collaboration and leadership5
  • Regulatory submissions3
  • GMP and compliance1
  • Data and digital systems1
  • Clinical trial conduct1

Company hiring pulse

Iambic on Regulatory Jobs

7
Open roles
7
Distinct roles
2
Locations

By discipline

  • Clinical6 86%
  • Regulatory1 14%

By level

  • Director3 43%
  • Manager2 29%
  • Senior & Principal2 29%
See all 7 Iambic roles

More roles at Iambic

All 7 Iambic roles

Similar Clinical Evaluation & Medical Writing roles elsewhere

Principal Medical Writer at Iambic

Open until filled. $152K–$190K a year, employer provided.

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