SystImmune is a leading and well-funded clinical-stage biopharmaceutical company located in Redmond, WA and Princeton, NJ. It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs). SystImmune has multiple assets in various stages of clinical trials for solid tumor and hematologic indications. Alongside ongoing clinical trials. SystImmune has a robust preclinical pipeline of potential cancer therapeutics in the discover and IND-enabling stages, representing cutting-edge biologics development. We offer an opportunity for you to learn and grow while making significant contributions to the company's success.
We are seeking a technically proficient and detail-oriented Safety Database Administrator to support our global pharmacovigilance (PV) operations. This role is critical to ensuring the integrity, security, and regulatory compliance of safety data related to our products. The successful candidate will work closely with the Senior Director of PV Operations and cross-functional teams to manage and optimize our safety database systems.
Key ResponsibilitiesPV Database Management & Configuration- Maintain and configure safety databases (e.g., ArisG, Argus, or similar) to support case processing, reporting, and compliance.
Data Integrity & Compliance- Ensure accuracy, completeness (experience with UAT testing), and regulatory compliance of safety data in accordance with global PV regulations (FDA, EMA, ICH, etc.).
System Integration & Automation- Support integration of the safety database with other systems (e.g., E2B gateways, regulatory submission platforms, signal detection tools) and drive automation initiatives.
User Support & Training- Provide technical support and training to PV users, troubleshoot issues, and manage user access and roles.
Reporting & Analytics- Generate and validate safety reports, metrics, and dashboards to support PV oversight and decision-making.
Qualifications- Bachelor’s degree in Life Sciences, Computer Science, or related field; advanced degree preferred.
- 3+ years of experience in safety database administration within a pharmacovigilance or drug safety environment.
- Hands-on experience with ArisG, Argus, or similar safety database platforms.
- Strong understanding of global PV regulations and compliance requirements.
- Excellent analytical, problem-solving, and communication skills.
- Experience with system validation, audit readiness, and documentation best practices.
Preferred Skills- Experience with database upgrades, migrations, and enterprise-level configurations.
- Familiarity with signal detection, risk management, and regulatory reporting tools.
- Knowledge of SQL, EXCEL, data visualization tools, and PV analytics platforms.
Compensation and Benefits:The expected base salary range for this position is
$70,000 - $100,000 annually. Actual compensation will be based on a variety of factors, including but not limited to a candidate’s qualifications, experience, and skills.
While most offers typically fall within the low to mid-point of the range, we may extend an offer toward the higher end for exceptional candidates whose background and expertise exceeds the requirements of the role.
SystImmune is a leading and well-funded biotech company with a bright future. We offer an opportunity for you to learn and grow while making significant contributions to the company’s success. SystImmune offers a comprehensive benefits package including: 100% paid employee premiums for medical/dental/vision, also STD, LTD, a 401(k) plan with a 50% company match of up to 3% and a vesting schedule of only 5 years, 15 PTO days per year, sick leave, plus 11 paid holidays and MORE.
We offer an opportunity for you to learn and grow while making significant contributions to the company’s success.
SystImmune is an Equal Opportunity Employer. We welcome diverse talent and encourage all qualified applicants to apply.