K

Keros Therapeutics

Develops TGF-ß signaling-modulating therapeutics

Director – Medical Affairs

Biology & BiotechConfirmed live in the last 24 hours
Full-timeLexington, MA, USA$225k - $257kHybrid

About the Job

Requirements

  • Strong foundational experience or exposure to patient advocacy management, with a genuine passion for supporting rare disease communities; neuromuscular or bone disease experience is a major plus.
  • Ability to work effectively with minimal structure, map out necessary processes, and independently prioritize deliverables in a lean environment.
  • Experience working with early-stage clinical assets and a strong understanding of the clinical development lifecycle.
  • Track record of building trusted, strategic relationships with key opinion leaders and external stakeholders.
  • Ability to manage multiple distinct therapeutic areas simultaneously while maintaining focus.
  • 5–8+ years of relevant experience within medical affairs in the biotech or pharmaceutical industry.

Responsibilities

  • Lead the medical affairs function, establishing short-term stabilization and creating a long-term roadmap to scale the team as clinical assets progress.
  • Serve as the primary liaison and strategic lead for patient advocacy groups across DMD, ALS, and bone disorders, fostering trusted, long-term external relationships.
  • Drive the development and execution of the scientific communications strategy, including managing medical publication planning, abstracts, and congress presentations.
  • Execute hands-on external engagement strategies by identifying, developing, and maintaining relationships with key opinion leaders and regional medical experts.
  • Act as the core medical affairs subject matter expert, partnering with Clinical Development, Clinical Operations, and Regulatory Affairs to support trial execution and insight generation.
  • Synthesize and communicate field-based medical insights to internal cross-functional teams to inform clinical strategy and program prioritization.
  • Manage external vendors, medical writing partners, and consultants supporting scientific communications and medical material generation to ensure high-quality deliverables.
  • Oversee the review and medical accuracy of scientific, regulatory, and corporate communication materials, ensuring compliance with relevant industry guidelines and standard operating procedures.

Desired Qualifications

  • Neuromuscular or bone disease experience.
  • An advanced scientific degree (MD, PhD, PharmD, or equivalent).
  • Individuals looking to take the next step in their career.

About the Company

Keros Therapeutics

Develops TGF-ß signaling-modulating therapeutics

Keros Therapeutics focuses on developing therapies that target the transforming growth factor-beta (TGF-ß) signaling pathway to treat diseases linked to its dysfunction. Its products aim to modulate TGF-ß signaling to influence cellular growth and repair, with the goal of altering disease progression and providing disease-modifying benefits, especially in blood cells and tissues. The company advances therapeutics through research and development, with commercialization as its end goal once therapies are approved for patients. What sets Keros apart is its specialized expertise in TGF-ß biology and its emphasis on creating drugs that directly modulate this signaling network to produce meaningful clinical outcomes. The overall goal is to bring therapies to market that improve patient outcomes by correcting or adjusting TGF-ß-related signaling in relevant diseases.

Company size
51-200
Company stage
IPO
Headquarters
Lexington, KY
Founded
2015

Recently Posted Jobs

Explore more opportunities at Keros Therapeutics

See more jobs