Scientist/Sr. Scientist, Clinical Pharmacology

Systimmune•Princeton, NJ

3d•$90,000 - $140,000•Onsite

About The Position

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 Scientist/Sr. Scientist, Clinical Pharmacology will support the design, execution, and analysis of clinical pharmacology studies to support drug development programs. This role will contribute to pharmacokinetics (PK), pharmacodynamics (PD), and regulatory strategy to optimize study design, data interpretation, and regulatory submissions. The successful candidate will be expected to both conduct hands-on PK/PD modeling and simulation and provide strategic leadership across programs. This role will collaborate cross-functionally to advance SystImmune’s pipeline of innovative oncology therapeutics and represent clinical pharmacology in regulatory interactions. It will be able to function in a blended role that includes both classical clinical pharmacology skillsets combined with quantitative analysis skills. This is a full-time onsite position at our Princeton, NJ location.

Requirements

Ph.D., Pharm.D., or equivalent with minimum 2 years of relevant experiences; or MS or equivalent with minimum 4 years of relevant experience; or equivalent level of expertise and experience.
Proficient in developing NCA analysis, PopPK, PK/PD, ER analysis, model informed drug development (MIDD) principles, and data visualization, results interpretation and reporting.
Proficiency in modeling software such as NONMEN, R, WinNonlin, Phoenix, etc.
Good knowledge and experience of drug development in one or multiple TAs. Critical thinking skills, with keen scientific and development judgment. Self-motivated performance and working on teams and in a matrix environment.
Ability to multi-task and prioritize assignments, establishing courses of action for self and others to ensure that work is completed efficiently and in a timely manner
Ability to work independently and collaboratively in a multidisciplinary team.
Strong problem-solving skills and ability to meet deadlines in a fast-paced environment.
Excellent communication, presentation, and interpersonal skills.

Nice To Haves

Postdoctoral experience, hospital experience, and industry experience are preferred.

Responsibilities

Responsible for clinical development strategy, clinical study design/protocol development, and documentation from CP perspective in the assigned project(s):
Contributes to clinical development strategies of pipeline products across various therapeutic areas and design of clinical studies with some supervision under supervision
Collaborate closely with preclinical, clinical, regulatory, biostatistics, and medical affairs teams to drive drug development programs and contribute to trial designs, dosing strategies, and regulatory submissions and interactions with health authorities.
Lead the design, validation, and implementation of pharmacometric models to inform decision-making at various stages of drug development.
Responsible for Pharmacometrics development, PK and PK/PD analysis, and documentation:
Conduct modeling and simulation work on PopPK, ER, PK/PD or exploratory analyses and guides PK/PD modeling or simulations as appropriate and to guide study design, inform dose selection and optimization, and efficacy/safety assessments.
Contributes to and owns modeling and simulation plan and prepare submission packages
Utilize modeling software such as NONMEM®, R, or other relevant tools to perform data analysis and generate modeling results.
Manages data analysis, interpretation, and reporting with some supervision
Evaluates and applies new data and data analyses to refine studies in the development plan
Stay current with the latest advancements in pharmacometric methodologies, applying innovative techniques to enhance modeling practices.
Integrates all available data (both clinical and nonclinical data) to clinical development strategy from CP point of view
Mentor and guide junior pharmacometricians, fostering a culture of continuous learning and development within the team.
Responsible for clinical pharmacology data package for NDA and responding to regulatory authority queries in the assigned project(s)
Carry out functional responsibilities in accordance with applicable SOPs and regulatory requirements