Scientist II in Vivo Scientist in Chronic Kidney Disease Research

Spectraforce Technologies, Inc.; Ridgefield (CT); Presencial; USD 75 000 - 105 000; Tempo integral

Resumo da oferta

Spectraforce Technologies, Inc. is seeking a Scientist II in Vivo CKD research based in Ridgefield, CT. You will initiate and complete routine CKD in vivo studies with minimal supervision and interpret results to guide follow‑up experiments.

You will design non-routine CKD/CRM in vivo experiments, ensure IACUC compliance, maintain accurate records, and communicate findings clearly in reports and protocols. A Master's or Bachelor's with 3+ years in related science is preferred.

Qualificações

• Hands-on in vivo CKD research with rodent models.
• Experience with rodent dosing and health monitoring.
• IACUC compliance experience.
• Proven problem-solving and agile learning.
• Ability to work in a collaborative environment.
• Strong data interpretation and reporting skills.

Responsabilidades

• Initiate and complete routine in vivo CKD studies with minimal supervision.
• Assist design and execution of non-routine CKD/CRM in vivo experiments.
• Ensure IACUC compliance and maintain proper records.
• Perform literature searches and extract protocol information.
• Operate lab equipment and troubleshoot as needed.
• Prepare and contribute to scientific reports and protocols.
• Report data with integrity and adhere to ethics.

Conhecimentos

In vivo studies

CKD models

Data analysis

Collaboration

Problem solving

Literature searches

Communication

Formação académica

Master's or Bachelor's in related field

Ferramentas

Excel

GraphPad Prism

Descrição da oferta de emprego

Position Title: Scientist II in Vivo Scientist in Chronic Kidney Disease Research

Work Location: Ridgefield, CT 06877

Assignment Duration: 12 Months

Work Schedule: Recurring weekend to support business operations. Scheduling is flexible and would not be every weekend. As needed, integration into weekend/holiday rotation at a cadence consistent with the rest of the team.

Work Arrangement: Onsite

Position Summary

• Initiates and completes routine in vivo studies, principally in field of chronic kidney disease (CKD), in an independent and efficient manner, with minimal supervision.
• Demonstrates the ability to interpret outcome of experiments and to propose appropriate follow-up; troubleshoots effectively.

Key Responsibilities

• Initiates and completes routine in vivo studies, principally in field of chronic kidney disease (CKD), in an independent and efficient manner, with minimal supervision. Demonstrates the ability to interpret outcome of experiments and to propose appropriate follow-up; troubleshoots effectively
• Demonstrates technical ability to assist in the design and execution of non-routine experiments in the context of CKD and cardio-renal-metabolic (CRM) in vivo models; conducts exploratory experiments with minimal supervision.
• Complies with applicable regulations including IACUC governance, performing all work in a safe and compliant manner; maintains proper records in accordance with Standard Operating Procedures and policies.
• Applies basic scientific principles for study design, data analysis, and interpretation; performs literature searches and extracts relevant information from published protocols.
• Independently operates and is responsible for lab equipment; troubleshoots effectively.
• Communicates own work effectively orally and in writing; contributes to writing protocols and procedures; provide input for scientific reports.
• Reports and treats data with a high level of integrity and ethics.

Qualification & Experience

• Apply knowledge of basic theory and scientific principles of to conduct hands‑on in vivo research; direct experience in rodent models of CKD is desirable.
• Experience in routine routes of rodent dosing (I.V., I.P., P.O., S.C., and I.M.), health monitoring, and sample collection is required.
• Compliance and communication experience with IACUC governance.
• Proven problem-solving ability with aptitude for agile learning style.
• Assist in the incorporation of new technologies to enhance cardio-renal-metabolic research.
• Proficiency with data analysis software such as Microsoft Excel and GraphPad Prism; expectation to develop expertise in other software, as necessary.
• Ability and willingness to work effectively in a highly collaborative environment.
• Master's Degree or Bachelor's Degree with 3+ years experience in related scientific discipline; pharmaceutical, biotechnology or CRO experience is highly desirable; non-PhD applicant required.