Pharmacovigilance Scientist

Oruka Therapeutics is seeking a Pharmacovigilance Scientist to collect, evaluate, and manage drug safety data throughout clinical development. The role supports the monitoring and assessment of adverse events, safety signal detection, and risk management activities to safeguard patient safety and ensure regulatory compliance.

Requirements

• Advanced degree in life sciences (e.g., PharmD, PhD) or related field
• Minimum of 3 years of experience within the pharmaceutical industry, ideally including drug safety experience
• Knowledge of good pharmacovigilance practices, drug safety regulations, and clinical trial processes
• Understanding of pharmacovigilance regulatory practices including CIOMS, EMA, ICH and FDA guidelines
• Experience with adverse event data review, safety signal detection, and safety database management (e.g. Argus, MedDRA, Veeva Vault)
• Strong analytical, communication and presentation skills
• Strong organizational and project management skills
• Ability to collaborate effectively across multidisciplinary teams in a fast-paced environment

Benefits

• Competitive salary and benefits package
• Supportive and inclusive team environment
• Opportunities for professional growth and development