Job description for an immunotoxicology research scientist in a contract research organization (CRO):

Responsibilities

• Conduct and oversee immunotoxicology studies, ensuring high-quality data interpretation, integration, and risk assessment to support product safety and inform dose selection for clinical investigations or regulatory submissions.
• Perform sample analysis for blood and urine clinical pathology using ADVIA 120 Hematology system (Siemens Diagnostics); coagulation (STA Compact Max3 analyzer and clinical chemistry (VITROS® XT 3400 analyzer ).
• Perform sample analysis using various assays and techniques such as ELISA, ECL, cell culture, PBMC extraction, and flow cytometry.
• Review and interpret study data to prepare high-quality reports.
• Serve as a subject matter expert in immunology/immunotoxicology, providing guidance on safety-related regulatory issues, formulation selection, and program development strategies.

Qualifications

• PhD, Master’s Degree or experience in a related field (e.g., immunology, toxicology) with typically 5+ years of relevant work experience.
• Strong background in immunology, immunotoxicology, and/or preclinical toxicology, preferably in a CRO or regulatory research setting.
• Expertise in clinical pathology and various immunological assays and cellular techniques, including flow cytometry, FACS, and immunophenotyping.
• Excellent understanding of the drug development process and knowledge of relevant regulations.
• Strong interpersonal, organizational, and communication skills.
• Ability to work effectively in a matrix organization and collaborate with diverse groups.

Benefits of Working in a CRO

Working in a contract research organization can offer several advantages for an immunotoxicology research scientist:

• Diverse Experience: CROs work on a variety of projects across different therapeutic areas, providing exposure to a wide range of drug development programs.
• Stability: CROs often offer more job stability compared to traditional pharmaceutical companies or biotech startups.
• Career Growth: There are opportunities for advancement from technician to scientist and management roles.
• Skill Development: CROs value a broader skillset, allowing scientists to develop expertise across multiple disease indications and research areas.
• Industry Exposure: Working in a CRO provides insights into various pharmaceutical and biotech companies’ research programs and strategies.

This role combines scientific expertise with regulatory knowledge to ensure the safety and efficacy of new drugs and therapies, particularly focusing on their effects on the immune system. It offers a challenging and rewarding career path for those interested in immunotoxicology and drug development.
Job Type: Full-time
Pay: $65,000.00-$75,000.00 per year

Benefits:

• Dental care
• Disability insurance
• Life insurance

Schedule:

• Monday to Friday
• Overtime

Work Location: In person
Application deadline: 2025-04-30
Expected start date: 2025-04-1

• Conduct and oversee immunotoxicology studies, ensuring high-quality data interpretation, integration, and risk assessment to support product safety and inform dose selection for clinical investigations or regulatory submissions.
• Perform sample analysis for blood and urine clinical pathology using ADVIA 120 Hematology system (Siemens Diagnostics); coagulation (STA Compact Max3 analyzer and clinical chemistry (VITROS® XT 3400 analyzer ).
• Perform sample analysis using various assays and techniques such as ELISA, ECL, cell culture, PBMC extraction, and flow cytometry.
• Review and interpret study data to prepare high-quality reports.
• Serve as a subject matter expert in immunology/immunotoxicology, providing guidance on safety-related regulatory issues, formulation selection, and program development strategies