Senior Manager, Pharmacovigilance Safety Operations

Senior Manager, Pharmacovigilance Safety Operations Employer Alumis Inc. Location South San Francisco Start date Apr 1, 2026 View more categories View less categories Discipline Administration , Clinical , Drug Safety/Pharmacovigilance Required Education Bachelors Degree Position Type Full time Hotbed Biotech Bay Apply now Save job Click to add the job to your shortlist You need to sign in or create an account to save a job. Send job Job Details Company Job Details Alumis Inc. is a precision medicines company with the mission to transform the lives of patients with autoimmune diseases. Even with treatment innovations of the last two decades, many patients with immunologic conditions continue to suffer - our goal is to fundamentally change the outcomes for these patients. Senior Manager, Pharmacovigilance Safety Operations The Senior Manager, Pharmacovigilance (PV) Safety Operations will report to the Director, PV Safety Operations. This role will play a critical role in ensuring timely reporting, processing, and submission of ICSRs from ongoing clinical trials and post-marketing trials. This role involves overseeing case processing vendors, managing ICSR process, collaborating with cross-functional teams study execution teams, assisting with inspection readiness activities, all while compliance with regulatory requirements. Essential Responsibilities ICSR Operational Excellence/Vendor Oversight

• Provide end-to-end operational oversight of ICSR intake, processing, follow-up, quality control, and submissions performed by our outsourced PV vendors.
• Ensure accurate and timely processing of ICSR to ensure accuracy and consistency, and compliance with Alumis standard operating procedures (SOP) and PV system expectations.
• Lead the development and maintenance of safety management plans and submission tracking systems.
• Support the development and maintenance of SOPs.
• Coordinate internal medical review activities in collaboration with medical case reviewers.
• Monitor case flow to ensure timely exchange for submissions.
• Review operational trends and quality indicators to proactively identify risks and drive corrective actions.
• Collaborate with clinical operations, data management, and PV teams to perform database reconciliation for clinical trials.
• Track the submission of safety reports to regulatory authorities and ensure compliance with country or regional submission deadlines.
• Ensure all safety operations are conducted in compliance with FDA, ICH, and other relevant regulatory guidelines. Cross-Functional Collaboration
• Work closely with clinical development, regulatory, and quality assurance teams to align safety operations with overall study objectives and ensure regulatory compliance.
• Assist in the preparation of new clinical trials study start up activities such as review Safety sections of clinical trial protocols, Informed Consent Forms, clinical database configurations, including User Acceptance Testing and Safety Case Report Forms.
• Collaborate with Safety Surveillance and assist in the preparation of surveillance meeting materials from safety operation perspective and assist with the development of aggregate reports, such as Development Safety Update Report (DSUR), Periodic Adverse Drug Experience Report (PADER), Periodic Benefit-Risk Evaluation Report (PBRER) by performing various activities such as quality control.
• Contribute to PV system audit-readiness and support inspections activities. The Ideal Candidate
• Bachelor's degree in life sciences, pharmacy, or a related field.
• Minimum of 7+ years of experience in safety operations in the biopharmaceutical industry.
• Experience with early and late-stage clinical trials (Phase 3) and post-marketing are highly desirable.
• Experience with device safety reporting and regulatory inspections is a plus.
• Strong knowledge of regulatory requirements (e.g., FDA, ICH guidelines) and industry standards related to drug safety and case processing.
• Demonstrated experience in vendor oversight, submission tracking, and quality control.
• Excellent organizational, analytical, and communication skills.
• Ability to work independently and collaboratively in a fast-paced environment and manage multiple projects simultaneously.
• Leads self by managing and executing own work to deliver results that contribute to accomplishing common department goals
• Proficiency in safety databases and software tools (e.

g., Oracle Argus, ARISg, MedDRA). This role is anchored at our South San Francisco, CA headquarters, with an expectation to be onsite Tuesday through Thursday. While we prefer local candidates, remote applicants based in the Pacific Time Zone will be considered on a case-by-case basis with the ability to travel to HQ approximately once per month, or as business needs require. The salary range for this position is $170,000 USD to $200,000 USD annually. This salary range is an estimate, and the actual salary may vary based on the Company's compensation practices. Company Alumis Inc. is a precision medicines company with the mission to transform the lives of patients with autoimmune diseases. Our experienced leadership team brings a proven track record in precision drug development of groundbreaking therapies. Even with treatment innovations of the last two decades, many patients with immunologic conditions continue to suffer. With a unique precision analytics platform and an unwavering commitment to advancing our understanding of immunologic diseases, Alumis Inc. will rewrite the autoimmune treatment playbook by developing the right medicine for each patient.

Company info Website http:

//www.alumis.com/ Location 611 Gateway Blvd Suite 820 South San Francisco California 94080 US Share this job Facebook Twitter LinkedIn Apply now Send job Apply now Save job Click to add the job to your shortlist You need to sign in or create an account to save a job. Get job alerts Create a job alert and receive personalized job recommendations straight to your inbox. Create alert