PV Operations Specialist

Posted 4 Days Ago
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Princeton, NJ, USA
In-Office
85K-115K Annually
Mid level
Biotech • Pharmaceutical
The Role
The PV Operations Specialist oversees pharmacovigilance operations, including safety case processing, regulatory submissions, and maintaining data integrity while collaborating with internal and external stakeholders.
Summary Generated by Built In
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.

Top Skills

Ema Regulations
Fda Regulations
Ich Guidelines
Pharmacovigilance
Safety Databases
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The Company
HQ: Redmond, Washington
83 Employees
Year Founded: 2014

What We Do

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 biologics that work through systematic intervention on the solid tumor micro-environment, to either directly attack the tumor and/or to activate the immune system to attack the tumor. We are a group of highly experienced immuno-oncology scientists utilizing several technology platforms to develop world class advanced antibody-based drug therapies.

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