Associate Director/Director of Drug Safety at Systimmune

Princeton, New Jersey, United States -

Full Time

Start Date

Immediate

Expiry Date

11 Apr, 26

Salary

250000.0

Posted On

11 Jan, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Drug Safety, Pharmacovigilance, Medical Safety Assessments, Safety Surveillance, Risk Management, Oncology, Hematology, Regulatory Compliance, Aggregate Safety Reports, Clinical Trials, Medical Review, Safety Signals, Standard Operating Procedures, Vendor Management, Causality Assessments, Benefit-Risk Assessment

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. This individual is to lead medical assessment and interpretation of safety data from multiple sources, including clinical trials, and literature reports. The individual will be closely collaborating with cross functional teams in supporting all clinical development programs, regulatory filling, and global safety related activities. This individual will also support the clinical R&D team in the oversight of PV service vendors and partners and will need to maintain medical knowledge, as well as current knowledge of drug safety and pharmacovigilance regulations, pharmacovigilance practices, safety surveillance and risk-management practices. This role requires a full-time onsite presence at our Princeton, NJ location. Responsibilities Provide medical safety input and participate in safety surveillance activities (e.g., identification of safety signals and ensure timely assessment and communication of confirmed safety signals). Provide input in the generation of aggregate safety reports (e.g., DSURs, PADER, PBRER). Serve as a leading medical safety resource for the development and review of clinical trial protocols, informed consent forms (ICFs), investigator brochures (IBs) and Reference Safety Information (RSI). Collaborate with Medical Monitors and Clinical Research Scientists and vendor clinical staff as needed for ongoing clinical trials. Provide medical safety input in the development and/or updates of Risk Management Plans and the maintenance of these documents. Provide support and input to the development of Standard Operating Procedures, Working Instructions, and other guidance documents. Serve as a subject matter expert for vendors that provide drug safety and pharmacovigilance services. Work closely with other Product Safety Leads to respond to and resolve safety questions from health authorities as well as regulatory agency’s audits and inspections. Qualifications 5+ years’ experience in Drug Safety/Pharmacovigilance in a pharmaceutical or biotech company, CRO or regulatory agency. Medical Degree (MD) from a recognized medical school with medical practice experience. Oncology / Hematology experience strongly preferred. Strong working knowledge of US and EU drug safety and pharmacovigilance regulations, CIOMS and ICH guidelines. Proven experience in medical safety assessments, safety surveillance and risk management activities. Proficiency with medical review of ICSRs, including expectedness assessments, causality assessments, narrative review and generation of Analysis of Similar Event and company comment statements, including benefit-risk assessment. Experience with preparation of aggregate reports (e.g., DSUR, PSUR/PBRER, PADER) Experience in preparation of responses to regulatory authorities; experience with regulatory filing and related activities preferred. Compensation and Benefits: The expected base salary range for this position is $150,000 - $250,000 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

The individual will lead medical assessment and interpretation of safety data from multiple sources, including clinical trials and literature reports. They will collaborate with cross-functional teams to support clinical development programs and regulatory activities.