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Senior Associate, Medical Safety Operations

Job in Foster City, San Mateo County, California, 94420, USA
Listing for: Mirum Pharmaceuticals, Inc.
Full Time position
Listed on 2026-01-12
Job specializations:
  • Healthcare
    Data Scientist
Salary/Wage Range or Industry Benchmark: 146000 - 151000 USD Yearly USD 146000.00 151000.00 YEAR
Job Description & How to Apply Below
Senior Associate, Medical Safety Operations

Foster City

Mission

Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. We are collaborative, creative, and experienced professionals and we’re looking to augment our team with other individuals who embody our values: care, be real, get it done, and have fun, seriously.

Position Summary

The Senior Drug Safety Associate in Medical Safety Operations will support vendor oversight activities with respect to the individual case safety report (ICSR) management process at Mirum.

Responsibilities
  • Perform routine retrospective quality review of the safety data collected to ensure completeness and accuracy. Collaborate with the pharmacovigilance (PV) vendor to address case corrections and trends.
  • Provide case processing guidance to the PV vendor in alignment with existing Mirum standards.
  • Review case metrics to ensure cases processed by the PV vendor are processed and exchanged within the agreed upon timelines.
  • Oversee and support reconciliation of safety data from various sources.
  • Oversee submission of expedited safety reports by the PV vendor and clinical contract research organizations; escalate and document late regulatory authority submissions.
  • Generate listing from Safety Database (Argus) or OBIEE as needed.
  • Responsible for interdepartmental collaboration, such as, but not limited to Quality Assurance, Clinical Operations, Regulatory Affairs on obtaining additional information as needed by PV vendor.
  • Manage and/or support system access (e.g. EDC, Argus etc.) along with periodic review of user access.
Education/Experience
  • Minimum of 3 years direct pharmaceutical industry experience dealing with global clinical study individual case safety report processing and reporting preferred; post-approval safety experience highly desired.
  • Detailed knowledge of relevant US, EU, and ICH guidelines, initiatives and regulations governing both clinical studies and post-approval safety.
Knowledge,

Skills and Abilities
  • Bachelor’s degree in life sciences.
  • Safety database experience is required.
  • Proficient in MS Word, Excel, PowerPoint, Outlook, and other applicable business software tools.

The salary range for this position is $146,000 to $151,000 USD. Compensation will be determined based on several factors including, but not limited to; skill set, years of experience, and the employee’s geographic location. Please note that the required compensation details listed in US role postings reflect the base salary only, and do not include bonus, equity, or benefits unless otherwise provided.

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Equal Employment Opportunity

Mirum Pharmaceuticals is committed to Equal Employment Opportunity (EEO) and to compliance with all Federal, State and Local laws that prohibit employment discrimination on the basis of race, age, national origin, ethnicity, religion, gender, gender identity, pregnancy, marital status, sexual orientation, citizenship, genetic disposition or characteristics, disability, veteran’s status or any other classification protected by applicable State/Federal/Local laws.

Mirum Pharmaceuticals provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in job application procedures.

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Position Requirements
10+ Years work experience
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