Senior Manager, Program Leadership - Waltham, United States - Lyra Therapeutics

Description

Lyra Therapeutics, Inc.

is a clinical-stage biotechnology company developing novel, integrated drug and delivery solutions for the localized treatment of patients with chronic rhinosinusitis (CRS) and other chronic diseases.

Lyra has two investigational product candidates, LYR-210 and LYR-220, in late-stage development for CRS, a highly prevalent inflammatory disease of the paranasal sinuses which leads to debilitating symptoms and significant morbidities.

LYR-210 and LYR-220 are bioresorbable polymeric matrices designed to be administered in a brief, non-invasive, in-office procedure and are intended to deliver up to six months of continuous mometasone furoate drug therapy to the sinonasal passages as an alternative to sinus surgery.

LYR-210 is designed for surgically naive patients and is being evaluated in the ENLIGHTEN Phase 3 clinical program, while LYR-220, an enlarged matrix, is being evaluated in patients who have recurrent symptoms despite surgery in the BEACON Phase 2 clinical trial.

These two product candidates are designed to treat the estimated four million CRS patients in the United States who fail medical management each year.

We are currently seeking a Senior Manager/ Associate Director, Program Leadership to manage the operational planning, and cross-functional communication for our two lead drug development programs.

The Senior Program Manager will work with the Program Leads to manage the Companys program management planning capability and tools in order to enhance the efficiency and effectiveness of Lyras program teams.

This position reports to the Associate Vice President, Program Leadership and will work closely with the Program Development Team and Program Development Sub-Teams to manage program activities.

One of the main responsibilities initially will be managing the cross-functional activities to ensure a successful and timely NDA submission.

The ideal candidate is an experienced program manager with 8 or more years of experience in drug and/or combination drug-device development.

Key Areas of Responsibility:
Work with Program Lead and Program Teams to build and maintain project plans for our two lead programs using MS Project or other project management tools
Work with Program Team in the preparation of agendas, meeting minutes, presentation materials, and follow up action items
Maintain tools for communication about project goals and progress (i.e. Egnyte, Office 365 sites)
Track progress of activities and deliverables, manage key program deliverables, and identify program risks and mitigation strategies, and anticipate potential issues
Develop and maintain key program tracking tools for communication with the Senior Leadership Team
Work with the Program Team and Finance to define budgeting and forecasting information utilizing the financial management system
Manage the cross functional NDA deliverables
Support the Program Lead in management of projects to support the Program Management function
Support the development of Program Integrated Development Plans and annual 5-year Long Range Plan


Qualifications:
Bachelors Degree or higher in a scientific discipline preferred
8+ years of product development program management experience in the pharmaceutical industry
Proven success working in cross-functional teams in a fast paced, entrepreneurial environment
Experience with program management for NDA submissions and familiarity with NDA components
Experience with cross-functional drug development process from clinical phase through commercialization. Medical device development experience is also a plus
Skilled in project management software
Effective communicator with exceptional written and oral communication skills

At Lyra, we value creativity, leadership, and collaboration.

The company sees significant expansion opportunities as we near commercialization, and look for people who are results-focused, innovative, and adaptable.

For consideration, please submit cover letter and CV. Please visit

for more information.
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