Senior Medical Director, Pharmacovigilance and Safety at Oruka Therapeutics in Waltham, MA

  • Company: Oruka Therapeutics
  • Location: Remote | Waltham, Massachusetts, United States
  • Salary: $306K – $343K
  • Job type: full time
  • Workplace: remote
  • Posted: 2026-09-25

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Job description

About Us: Oruka Therapeutics (Nasdaq: ORKA) is developing novel biologics designed to set a new standard for the treatment of chronic skin diseases. Oruka’s mission is to offer patients suffering from chronic skin diseases like plaque psoriasis the greatest possible freedom from their condition by achieving high rates of complete disease clearance with dosing as infrequently as once or twice per year. Oruka is advancing a proprietary portfolio of potentially best-in-class antibodies that were engineered by Paragon Therapeutics and target the core mechanisms underlying plaque psoriasis and other dermatologic and inflammatory diseases. For more information, visit www.orukatx.com As we build our core team, we're seeking top talent in different functional areas who are not just looking for a job, but an opportunity to be part of something bigger. Someone who is passionate about making a difference and eager to contribute to establishing an engaged, inclusive, and positive company culture. Job Title: Senior Medical Director, Pharmacovigilance and Safety Location: Remote or Hybrid if located near Waltham, MA office and will be required to be in-office in 3 days/week. Role Overview: Oruka is seeking an experienced, collaborative pharmacovigilance leader to provide medical and scientific safety oversight for Oruka’s investigational products. The Senior Medical Director, Pharmacovigilance and Safety will lead safety activities and processes, oversee Oruka’s pharmacovigilance vendors, and ensure continuous assessment of each product's safety profile and benefit-risk balance. This role will also serve as the medical safety expert on cross-functional development teams, working closely with internal and external stakeholders to ensure compliance with regulations and guidelines, contribute to safety regulatory documents, and protect participant safety. The successful candidate will combine strong clinical judgment and pharmacovigilance expertise with a team-oriented approach suited to a growing biotechnology company. The role will also help develop Oruka’s pharmacovigilance infrastructure, processes, governance, and vendor partnerships as the portfolio advances through clinical development and toward registration. Key Responsibilities: Product Safety Leadership and Risk Management Develop and lead product safety surveillance strategies, identify emerging clinical safety issues, and recommend appropriate risk-mitigation measures. Conduct or oversee routine and ad hoc reviews of safety data, monitor for safety signals, and maintain awareness of relevant drug-class and competitor safety issues. Lead ongoing aggregate safety review and chair internal safety governance committees. Plan and interpret safety data analyses; prepare and present safety data summaries to internal and external stakeholders. Build effective working relationships with clinical study teams, safety vendors, and business partners to align on product safety strategy. Medical Safety Oversight Oversee expedited safety reporting, including medical review of Individual Case Safety Reports (ICSRs), suspected unexpected serious adverse reactions (SUSARs), and other reportable safety events. Ensure appropriate medical follow-up and consistent medical assessment of individual safety cases. Provide medical review of clinical trial safety data, including adverse events, laboratory results, vital signs, ECGs, exposure data, and relevant nonclinical or external information. Provide medical safety guidance to investigators, study teams, and internal stakeholders. Clinical Development and Regulatory Support Lead safety-related aggregate reporting and the preparation and maintenance of relevant sections of Investigator's Brochures, including Reference Safety Information, Development Safety Update Reports, Risk Management Plans, and other regulatory documents. Provide safety input into clinical development plans, study protocols, informed consent forms, case report forms, statistical analys

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