Job Description

Job Summary:

We’re seeking an experienced Scientist to bolster our Clinical Pharmacology Lab team. Your primary role will be to spearhead PK and ADA assays using ELISA SoftMax Pro and MSD platforms. Additionally, you'll take charge of assay validation, tech transfer, and development, ensuring adherence to industry standards. Material management using LIMS software and maintaining GLP compliance will also be key aspects of your responsibilities.

Essential Duties and Responsibilities:

• Lead PK and ADA assays, ensuring strict adherence to protocols and SOPs.
• Drive assay validation, tech transfer, and development initiatives to maintain industry standards.
• Manage laboratory materials effectively through LIMS software, including inventory tracking and ordering.
• Maintain meticulous records of experimental procedures, results, and data analysis while troubleshooting assay issues as they arise.
• Collaborate closely with cross-functional teams to support research projects and mentor junior staff as needed.
• Stay abreast of emerging technologies and industry advancements to contribute to assay development and optimization.
• Assist in preparing regulatory documentation and participating in audits to ensure compliance with industry regulations.

Qualifications:

• Ph.D.; MS; BS in pharmaceutical or biotechnology industry; 5+ years with a focus on clinical pharmacology or bioanalytical assays.
• Proficiency in running PK and ADA assays using ELISA SoftMax Pro and MSD platforms.
• Strong organizational skills and attention to detail.
• Excellent communication and interpersonal skills for effective collaboration within multidisciplinary teams.
• Thorough understanding of GLP regulations and regulatory guidelines.
• Problem-solving abilities and a proactive attitude towards continuous improvement.
• Onsite work is mandatory.

Join us in advancing cutting-edge clinical pharmacology research and contribute your expertise to our dynamic team!

Physical Demands:

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.
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While performing the duties of this job, the employee is regularly required to sit for long periods of time. This individual must be able to operate standard laboratory and business equipment.

The hiring pay range for this position is $70,000 - $140,000 per year based on skills, education, and experience relevant to the role.

 

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 discovery or 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. SystImmune offers a comprehensive benefits package. 

SystImmune is an Equal Opportunity Employer. We welcome diverse talent and encourage all qualified applicants to apply.

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