
51 - 200 employees
Founded 2016
🏥 Healthcare
💼 Consulting
⚖️ Legal
Healthcare • Consulting • Legal
Immunic Therapeutics is a late-stage biotechnology company focused on developing novel, orally administered small-molecule therapies for chronic inflammatory and autoimmune diseases, with particular programs targeting multiple sclerosis and celiac disease. The company advances differentiated clinical-stage programs (e. g. , vidofludimus calcium, IMU-856, IMU-381) aiming to provide efficacious, safe, and well-tolerated oral treatment options for neurologic and gastrointestinal immune-mediated conditions, while pursuing regulatory protections and commercialization pathways.
🕒 6 days ago
🇺🇸 United States – Remote
💵 $180k - $230k / year
⏰ Full Time
🟠 Senior
👷♀️ Project Manager
👻 Ghost score 3%
Where this job comes from
Posted on Immunic Therapeutics's careers page, not through a job board
First seen by Remote Rocketship 6 days ago
Still open on Immunic Therapeutics's site. Checked 1 hour ago.

51 - 200 employees
Founded 2016
🏥 Healthcare
💼 Consulting
⚖️ Legal
Healthcare • Consulting • Legal
Immunic Therapeutics is a late-stage biotechnology company focused on developing novel, orally administered small-molecule therapies for chronic inflammatory and autoimmune diseases, with particular programs targeting multiple sclerosis and celiac disease. The company advances differentiated clinical-stage programs (e. g. , vidofludimus calcium, IMU-856, IMU-381) aiming to provide efficacious, safe, and well-tolerated oral treatment options for neurologic and gastrointestinal immune-mediated conditions, while pursuing regulatory protections and commercialization pathways.
• Serve as project manager for one or more development program sub-teams or strategic corporate initiatives • Drive execution against goals and proactively resolve delivery-impacting issues • Develop and maintain integrated cross-functional project plans with milestones, dependencies, assumptions and critical paths • Coordinate readiness for Phase 3 execution, data readouts, NDA preparation, regulatory interactions and launch planning • Facilitate collaboration among internal teams and external partners • Run governance meetings, steering committees and leadership reviews • Maintain action, decision and risk logs • Prepare updates, dashboards, risk assessments and decision materials for senior management • Escalate critical issues to support informed decision-making • Identify, assess and monitor risks and opportunities • Propose mitigation strategies and support scenario planning and evaluation of strategic alternatives • Partner with functional leaders on resource requirements, constraints and trade-offs • Apply and continuously improve project management standards, tools, governance, planning and reporting processes, including lessons learned
• 8-12+ years of experience • Bachelor's degree in Life Sciences, Pharmacy, Medicine, Business or a related discipline • Strong knowledge of clinical development processes from Phase 1 through Phase 3 • Knowledge of major regulatory submissions, including IND, NDA, MAA and BLA • Strong command of integrated planning, critical-path analysis, scenario planning, risk management, governance, budgeting and lifecycle management • Proven leadership of complex global cross-functional teams • Ability to influence without formal authority in a matrix environment • Ability to resolve conflict and manage senior stakeholders • Strong risk management and problem-solving capabilities • Demonstrated judgement, accountability and delivery focus while balancing speed, cost, quality and compliance • Excellent executive communication, facilitation, influencing and decision-support skills • Ability to operate effectively at strategic and hands-on levels in a dynamic matrix organization • PMP or comparable qualification preferred
• Equity • Bonus • Equal Opportunity Employer commitment to a diverse, inclusive, and equitable workplace
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