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Keros Therapeutics

Director, Program Management

Lexington, MA (Hybrid); Lexington, MA (Hybrid)Hybrid · United States
Director+ · Program Management
POSTED 6 NOV
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Role
4 days opentrue age
Posted 6 Nov
Payats field
$201k–239kposted
▲ +5% vs market median $210k
$165k$264k
Market p25–p75
$165k–$255k
Keros Therapeutics p25–p75
$224k–$264kn=8
United States · n=5765 · 365d to 10 Nov
CompanyKeros Therapeutics →
15open roles
Opened · 30d
+0
Closed · 30d
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30d window
Market
25,426open · Director+ Other
Opened · 7d
+1,7257% of open
All other
625,556open
All tracked boards · live 11 Nov · n=25,426

At Keros, our mission is to deliver significant clinical benefit to a wide range of patients with disorders that are linked to dysfunctional signaling of the transforming growth factor-beta (TGF-ß) family of proteins. With a focus on developing differentiated product candidates that are designed to alter TGF-β signaling, we aim to target the pathways critical for the growth, repair and maintenance of blood cells and a number of tissues, including bone, skeletal muscle, adipose and heart tissue. We believe our product candidates have the potential to unlock the full therapeutic benefits of modulating the TGF-β superfamily and provide disease-modifying benefit to patients.

Job Summary

The Director, Program Management, will provide strategic and operational leadership for the rinvatercept (KER-065) development program. This individual will lead cross-functional program planning and execution as rinvatercept advances through clinical development. The ideal candidate will combine strong drug-development program leadership with meaningful experience running clinical trials across Phase 1, Phase 2 and Phase 3.

The successful candidate will move effectively between strategic planning and hands-on execution, anticipate and mitigate risks, drive timely decisions and maintain alignment across Clinical Development, Clinical Operations, Regulatory Affairs, CMC/Technical Operations, Nonclinical, Biometrics and other functions.

Primary Responsibilities

Program Strategy and Leadership

  • Serve as the program management lead for rinvatercept, partnering with functional leaders to define and execute the optimal global development strategy
  • Lead the cross-functional program team, including representatives from Clinical Development, Clinical Operations, Regulatory Affairs, CMC/Technical Operations, Nonclinical, Biometrics, Medical Affairs, Commercial and Corporate Strategy
  • Guide the program through proof of concept, registration-enabling studies, regulatory submissions and potential marketing authorization
  • Translate development strategy into clear program objectives, operational priorities and measurable deliverables
  • Mobilize and align the organization around the program strategy and drive timely decision-making through appropriate governance forums
  • Balance day-to-day program execution with long-range strategic planning

Integrated Development Planning

  • Create and maintain an integrated strategic development plan covering program goals, value-creation milestones, critical-path activities, cross-functional dependencies, timelines, decision points, assumptions, risks, alternative scenarios, budget and resource requirements
  • Ensure functional plans are aligned with the overall development strategy and that interdependencies are clearly understood and actively managed
  • Identify potential gaps, conflicts and constraints before they affect clinical, regulatory or operational milestones
  • Lead scenario planning to evaluate alternative development approaches and their implications for timeline, resources, risk and program value

Clinical Development and Trial Execution

  • Partner with Clinical Development and Clinical Operations to plan and execute rinvatercept clinical trials across Phase 1, Phase 2 and Phase 3
  • Integrate clinical activities with regulatory, CMC, nonclinical, biometrics and other program workstreams
  • Identify and manage dependencies affecting protocol development, regulatory submissions, site activation, patient enrollment, study conduct, data delivery and clinical readouts
  • Support transitions between stages of development, including progression from early clinical studies into proof-of-concept and registration-enabling trials
  • Apply an understanding of neuromuscular and rare-disease trial challenges, including specialized investigator sites, patient recruitment, natural-history considerations, endpoints and global execution
  • Ensure clinical-trial plans are supported by realistic timelines, budgets, resources and risk-mitigation plans

Cross-Functional Team Effectiveness

  • Establish and lead an effective operating cadence for program team meetings, working sessions and governance reviews
Source · Keros TherapeuticsFirst seen 7 NovOriginal ↗