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In vivo Scientist

TechMind RPO


Job Location:

Ridgefield, CT - USA

Monthly Salary: Not provided by the employer
Posted: 6 October 2026 (3 days ago)
Application Deadline: 3 January 2027
Vacancies: 1 Vacancy

Job Summary

Responsibilities:

  • Excellent employment opportunity for a Scientist II in vivo Scientist in Chronic Kidney Disease researchin the Ridgefield CT area.
  • 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.
  • As needed integration into weekend/holiday rotation at cadence consistent with rest of the team
  • This role includes a recurring weekend to support business operations. Scheduling is flexible and would not be every weekend.

Experience:

  • Masters Degree or Bachelors Degree with 3 years experience in related scientific discipline; pharmaceutical biotechnology or CRO experience is highly desirable; non-PhD applicant required.
  • 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.