Director, Pharmacovigilance

Job not on LinkedIn

🕒 July 9

🇺🇸 United States – Remote

💵 $280k - $350k / year

⏰ Full Time

🔴 Lead

👔 Director

👻 Ghost score 26%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Immuneering Corporation

WebsiteLinkedInAll Job Openings

11 - 50 employees

Founded 2008

🏥 Healthcare

💼 Consulting

🎖️ Defense

💰 $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.

📋 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