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  3. Senior Pharmacovigilance Operations Specialist
Systimmune logo

Senior Pharmacovigilance Operations Specialist

Systimmune·Princeton, New Jersey

$85,000 - $115,000/yr·Full Time·Hybrid·2-5 yrs
·
Posted 13 days ago
Practice for this role

About the role

The role is responsible for end-to-end safety case processing, including intake, triage, and regulatory submissions. It also involves maintaining the PV database, managing CAPAs, and ensuring global compliance and inspection readiness.

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.

The PV Operations Specialist supports the Senior Director of Pharmacovigilance (PV) Operations in the oversight and execution of Systimmune’s global pharmacovigilance function. The position carries full accountability for end-to-end safety case processing, including regulatory submissions, hands-on work within the safety database, and CAPA management and coordination.

The incumbent is responsible for ensuring data integrity, optimal system performance, and compliance with global pharmacovigilance regulations and internal SOPs. The role requires close cross-functional collaboration with internal stakeholders and effective partnership with external vendors and service providers on pharmacovigilance-related activities.

This is an on-site position, requiring in-office presence a minimum of three days per week.

Key Responsibilities Perform intake, triage, data entry, and quality review of ICSRs.

Ensure timely regulatory submissions in accordance with global requirements.

Maintain accuracy and completeness of safety data in the PV database.

Collaborate with cross-functional teams to support audits, inspections, and CAPA implementation.

Follow SOPs, work instructions, and applicable regulations (e.g., FDA, EMA, ICH).

Support continuous improvement initiatives within PV operations.

Facilitate the generations of listings for the periodic safety reports (e.g., DSUR, PSUR).

Work with the QA department to maintain a state of high PV inspection readiness across all regions/countries.

Support the performance of root cause analysis of deviations relevant to PV systems.

Prepare responses to audit findings that concern the PV department.

Manage reconciliation activities with other departments within the company and vendors.

Qualifications

Bachelor’s degree in life sciences, pharmacy, nursing, or related field. 3-5+ years of experience in pharmacovigilance case processing preferred. Familiarity with safety databases (e.g., ArisG, Argus) and regulatory reporting requirements. Strong attention to detail, organizational skills, and ability to work independently.

Compensation and Benefits

The expected base salary range for this position is $85,000 - $115,000 annually. Actual compensation will be based on a variety of factors, including but not limited to a candidate’s level 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.

Requirements

Requires a Bachelor's degree in life sciences, pharmacy, nursing, or a related field. Preference is given to candidates with 3-5+ years of experience in pharmacovigilance and familiarity with safety databases like ArisG or Argus.

  • bachelor degree
  • Vendor Management
  • Compliance Monitoring
  • Root Cause Analysis
  • Data Integrity
  • Cross-functional Collaboration
  • Regulatory Submissions
  • Quality Review
  • Audit Readiness
  • CAPA Management
  • Safety Database Management
  • Pharmacovigilance Case Processing
  • ICSR Triage

Posting details

Employment type
Full Time
Work arrangement
Hybrid
Experience
2-5 yrs
Salary
$85,000 - $115,000/yr
Location
Princeton, New Jersey
Posted
Jul 15, 2026
Closes
Oct 13, 2026
Application
Employer website
Systimmune logo

Hiring organization

Systimmune

Located in Redmond WA, founded in 2014, Systimmune Inc. is a bio-pharmaceutical company focused on the treatment of cancer through developing novel therapeutic bi-specific, and tri-specific antibodies, as well as antibody-drug conjugates (ADC's). Our objective is to create...

Salary listed on 4 jobs
IndustryBiotechnology Research
TypePrivately Held
Size51-200 employees
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Market context

Operations roles in New Jersey are steady

Operations roles in New Jersey often see steady demand in settings that support daily service delivery, especially when reliability, scheduling, and compliance matter. These positions can be competitive because employers often look for candidates who already hold CPR/First Aid certification, have a high school diploma or GED, and can work well with seniors. Review the AI-summarized requirements and benefits here to save time, then confirm your certifications and highlight any senior-care experience before applying.

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