Manager/Senior Manager, PV Operation at Systimmune

Princeton, New Jersey, United States -

Full Time

Start Date

Immediate

Expiry Date

04 Mar, 26

Salary

150000.0

Posted On

05 Dec, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Pharmacovigilance, Drug Safety, Quality Management, Compliance, Safety Data Exchange, Adverse Event Processing, Signal Detection, Risk Management, Regulatory Inspections, Project Management, Training, Mentoring, Data Entry, Coding Review, Narrative Writing, Continuous Improvement

Industry

Biotechnology Research

Description

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 Manager or Senior Manager, Pharmacovigilance (PV) Operations to support the Senior Director of PV Operations in key areas of the pharmacovigilance function. This role will have accountability for vendor oversight, training, business process integration, Quality Management System (QMS) activities, Safety Data Exchange Agreements (SDEAs), safety database management, and CAPA coordination. This individual will manage the day-to-day operational activities of SystImmune’s Pharmacovigilance function, ensuring that all projects adhere to standard operating procedures (SOPs), internal policies, industry best practices, and applicable global regulations. The role will also work cross-functionally with internal teams and key stakeholders, as well as external partners, to support a wide range of pharmacovigilance-related activities. Responsibilities Coordinate the daily management and execution of drug safety (DS) and pharmacovigilance (PV) operations. Work with compliance with regulations, PV agreements, and internal SOPs. Represent the Drug Safety and Pharmacovigilance departments on clinical development teams. Oversee SAE (Serious Adverse Event) processing by outsourced vendors, and review and monitor compliance operations. Execute strategies to achieve and maintain the desired level of quality including, by analyzing and mitigating compliance risk. Process SAEs include case triage, data entry, coding review and narrative writing. Provide safety operations support for external submissions, signal detection, and risk management planning activities. Facilitate the preparation of periodic safety reports (e.g., DSUR, PSUR). Ensure compliant exchange of safety data between SystImmune and its partners. Work with the quality management system in Drug Safety to ensure department standards are met, including training requirements, monitoring performance, implementing continuous improvement actions, and good documentation practices. Work with the QA department to maintain a state of high PV inspection readiness across all regions/countries. Collaborate with contract service providers for case processing, aggregate reporting, and quality management activities. Conduct performance management of PV systems. Support the performance of root cause analysis of deviations relevant to PV systems. Participate in regulatory inspections and company audits including FDA/MHRA/EMA PV inspections. Prepare responses to audit findings that concern the PV department. Manage reconciliation activities with other departments within the company and vendors. Provide project management support to the NDA/MAA submission activities and prepare safety data submission. Support the cross - functional teams in patient narratives efforts. Participate in the bid defense process. Provide strategic oversight of vendors. Manage both quality and compliance of assignments, including training and mentoring. Qualifications Bachelor’s degree in healthcare or a BSN/RN degree with a minimum of 5-7 years pharmacovigilance experience in a pharmaceutical, biotechnology or related environment. An RPh, PharmD, or PhD degree may be considered with 3 years of relevant experience. At least 3 years minimum of experience in the following areas: Managing daily execution of pharmacovigilance (PV) operations Processing SAEs including case triage, data entry, coding review and narrative writing Providing drug safety operations support for external submissions, signal detection, and risk management planning activities Working with Drug Safety quality management systems to ensure compliance with department standards and training requirements, monitoring performance, implementing continuous improvement actions, and ensuring good documentation practices Overseeing compliance with Pharmacovigilance (PV) regulations, PV agreements, and internal SOPs, including analyzing and mitigating compliance risk, providing safety operations support for external submissions, signal detection, and risk management planning activities Preparing safety reports (e.g., DSUR, PSUR) Conducting performance management of PV systems and performing root cause analysis of deviations relevant to PV systems Conducting regulatory DSPV inspections and company audits including MHRA/EMA PV inspections, and preparing responses to audit findings Providing strategic oversight of pharma industry CRO and/or CMO vendors, managing both quality and compliance, and providing training and mentoring Compensation and Benefits: The expected base salary range for this position is $90,000 - $150,000 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.

Responsibilities

Manage the day-to-day operational activities of SystImmune’s Pharmacovigilance function, ensuring compliance with standard operating procedures and global regulations. Oversee vendor operations, safety data management, and support cross-functional pharmacovigilance activities.