Research Associate III (JR227957)

ViziRecruiter,LLC.; New York (NY); On-site; USD 70,000 - 90,000; Full time

Job summary

A leading healthcare research organization is seeking a Research Associate in New York, NY. This role involves the development and validation of molecular, genomic, and proteomic assays, requiring both a PhD and MS, along with 1-3 years of relevant experience. The successful candidate will lead multi-omic projects, design experiments, and maintain accurate records while working in a collaborative laboratory environment. This position offers a chance to contribute to innovative research with a strong community health focus.

Qualifications

• PhD and MS are required.
• 1-3 years of related experience required.
• Experience with lab protocols and workflows.

Responsibilities

• Design and lead pilot studies for new technologies.
• Lead multi-omic assay projects.
• Develop laboratory workflows for sample analysis.
• Serve as a technical resource for lab members.
• Establish goals and carry out experiments independently.
• Keep accurate records of methods and data.
• Support exploratory experiments and validation studies.

Skills

Technical resource advising

Experimental design

Nucleic acids isolation

Sample analysis

Education

PhD

MS

Job description

Introduction

To heal, to teach, to discover and to advance the health of the communities we serve.

To learn more about the “Montefiore Difference” – who we are at Montefiore and all that we have to offer our associates, please click here.

Overview

The research associate will be responsible for the development verification and validation of various advanced research and translations assays involved in both molecular, genomic and proteomic research. They will also be involved in clinical diagnostic assay development of non-commercially available assays (Laboratory Developed Protocols) which include constitutional genetic testing for, somatic oncologic testing, or for the rapid diagnosis of infectious diseases at the MMC clinical laboratories.

Responsibilities

• Design and lead pilot studies and explore new technologies with the potential to improve performance of existing products or open up new avenues of research and development.
• Lead multi-omic assay projects, potentially including whole genome, exome, targeted sequencing, methylation and/or proteomic methods
• Develop protocols and laboratory workflows to analyze samples, including isolation of nucleic acids (DNA/RNA) from banked biospecimens and QC.
• Serve as a technical resource for other lab members regarding advice on methods and experiment design and analysis.
• Establish experiment goals and plans, carry out experiments independently using standardized processes, including but not limited to DNA extractions, genomic sequencing library preparations, PCR, and quantity of samples.
• Keep an accurate record of all methods, observations, outcomes, and data generated, following the best practice in the team to collect and record data within LIMS, other IT application systems.
• May support exploratory experiments, validations, bridging studies, preparation of documentation for transitioning R&D protocol to clinical production.

Requirements

• PhD Required.
• MS Required.
• 1-3 years Required.
• OHS Fit Test.
• OHS Annual Assessment.