Senior Director, Safety and Pharmacovigilance

🕒 April 23

🏄 California – Remote

🏄 California – Remote

💵 $265k - $280k / year

⏰ Full Time

🟠 Senior

👔 Director

👻 Ghost score 10%

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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Artiva Biotherapeutics

WebsiteLinkedInAll Job Openings

51 - 200 employees

🧬 Biotechnology

🏥 Healthcare

💊 Pharmaceuticals

💰 Series B on 2021-02

Biotechnology • Healthcare • Pharmaceuticals

Artiva Biotherapeutics is an immunotherapy company dedicated to making safe and effective cell therapies accessible to any cancer patient who may benefit. The company specializes in producing off-the-shelf, allogeneic NK cell therapies at a massive scale. Its mission focuses on developing effective, safe, and accessible therapies for patients suffering from autoimmune diseases and cancers. Notably, their lead program, AlloNK®, is a non-genetically modified NK cell therapy candidate currently undergoing clinical trials for treatments of systemic lupus erythematosus and Non-Hodgkin Lymphoma, among others.

📋 Description

• Oversee global Safety and PV activities to ensure compliance with applicable regulatory requirements and guidances. • Oversee adverse event case processing (ICSRs) and aggregate reporting (DSUR) to ensure high-quality safety reports are submitted within required timelines to regulatory agencies and external stakeholders. • Lead the preparation and review of safety-related sections for clinical and regulatory documents. • Partner with Clinical Leads and Medical Monitors for medical review and reporting of individual adverse events and reactions, ensuring appropriate assessment of case seriousness, causality, expectedness, medical coding, and case follow-ups. • Serve as the primary liaison with internal departments and external partners on Safety and PV related issues. • Develop and update drug safety forms and templates, ensuring harmonization with clinical operation functions during study start-up and conduct of clinical studies. • Manage Safety and PV vendor relationships, execution of responsibilities, and ensuring compliance with safety data processing and submission activities. • Ensure effective serious adverse event (SAE) reconciliation between clinical and safety databases. • Develop and implement Safety and PV process improvements, tools, systems, and procedures. • Provide input into responses to regulatory inquiries and safety issues. • Contribute to the development and updates of safety documents, including core data sheets, investigator brochures, labels, and RMPs as required. • Participate in regulatory inspections and internal audits and author responses to findings. • Maintain close interactions and oversee the assessment and performance of assigned personnel, fostering an environment of professional development. • Able to work cross-functionally with other development and functional areas in the organization.

🎯 Requirements

• Minimum of 5 years of Drug Safety and PV experience in a biopharma or biotech organization • A health care professional background (e.g., MD, RN, BSN, PharmD, Physician Assistant) is required • Strong understanding of global Safety and PV regulations, including EU and US regulations and ICH guidelines • Excellent understanding of Good Pharmacovigilance Practices, GCP, clinical trial methodology, and medical terminology • Proficiency with safety databases (e.g. Argus), regulatory regulations, and MedDRA coding • Excellent interpersonal, organizational, and communication skills • Strong project management and problem-solving abilities • Attention to detail and quality-focused approach • Proven ability to prioritize workload and meet deadlines • Demonstrated initiative and flexibility through effective, innovative leadership • Strong negotiation and communication skills, with the ability to operate in a global, culturally diverse environment • Ability to work effectively both independently and in a team setting • Willingness to travel as required.

🏖️ Benefits

• Medical, Dental, and Vision • Group Life Insurance • Long Term Disability (LTD) • 401(k) Retirement Plan • Employee Assistance Program (EAP) • Flexible Spending Account (FSA) • Paid Time Off (PTO) • Company paid holidays, including the year-end holiday week • Recognition program, Bonus.ly