Immuneering Corporation
11 - 50 employees
Founded 2008
🏥 Healthcare
đź’Ľ Consulting
🎖️ Defense
🔥 Funding within the last year
đź’° $200M Post-IPO Equity - Immuneering on 2025-09
Healthcare • Consulting • Defense
Immuneering Corporation is a clinical-stage biotechnology company developing a novel class of oncology therapies called Deep Cyclic Inhibitors, which use rhythmic dosing to outpace cancer adaptation, improve tolerability, and extend patient survival and quality of life. The company advances a pipeline through clinical trials, collaborates with partners, and emphasizes scientific research and publications to transform cancer treatment while reducing side effects of traditional continuous-inhibition therapies.
Director, Pharmacovigilance
Job not on LinkedIn
đź•’ July 9
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Immuneering Corporation
11 - 50 employees
Founded 2008
🏥 Healthcare
đź’Ľ Consulting
🎖️ Defense
🔥 Funding within the last year
đź’° $200M Post-IPO Equity - Immuneering on 2025-09
Healthcare • Consulting • Defense
Immuneering Corporation is a clinical-stage biotechnology company developing a novel class of oncology therapies called Deep Cyclic Inhibitors, which use rhythmic dosing to outpace cancer adaptation, improve tolerability, and extend patient survival and quality of life. The company advances a pipeline through clinical trials, collaborates with partners, and emphasizes scientific research and publications to transform cancer treatment while reducing side effects of traditional continuous-inhibition therapies.
đź“‹ Description
• Build and lead the pharmacovigilance (PV) function at Immuneering • Oversee safety data management & reporting including ICSR processing and regulatory submissions • Establish formal signal detection and risk management processes • Collaborate with cross-functional teams including Clinical Operations and Regulatory Affairs • Manage vendor relations and ensure compliance with safety data obligations • Foster a culture of patient safety and prepare/manage a PV department budget
🎯 Requirements
• M.D. required • Minimum 5-8 years of pharmacovigilance experience in the biopharmaceutical industry, with at least 1 years in a leadership or director-level role • Demonstrated expertise in global PV regulations and guidelines (FDA 21 CFR Parts 312/314/600, EMA Good Pharmacovigilance Practice, ICH E2A/E2D/E2E/E6) • Experience overseeing all aspects of ICSR management, aggregate report authorship, and signal detection • Oncology drug development experience, including familiarity with oncology-specific safety profiles • Track record of successful health authority interactions on PV matters • Experience managing or overseeing PV safety databases (e.g., Argus, ARISg, Oracle LSH) • Strong scientific acumen with the ability to independently conduct and communicate benefit-risk assessments • Excellent written and verbal communication skills; ability to distill complex safety information for diverse audiences
🏖️ Benefits
• Competitive compensation • Equity participation • Exceptional benefits • Fully remote work environment • Flexible, results-oriented culture
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