Scientist - Clinical Research assumes lead role in various clinical research projects. Proposes, plans, organizes and executes experiments and research. Being a Scientist - Clinical Research secures grants and funding for research and is responsible for controlling budgets. Summarizes findings in reports and communicates results. Additionally, Scientist - Clinical Research interacts with other scientists within and outside of the organization. Provides recommendations that influence extensive clinical research activities. Requires an advanced degree. Typically reports to head of a unit/department. The Scientist - Clinical Research work is generally independent and collaborative in nature. Contributes to moderately complex aspects of a project. To be a Scientist - Clinical Research typically requires 4 -7 years of related experience. (Copyright 2024 Salary.com)
Clinical Research Scientist/Clinical Assay Developer
Job Description
Diagnostic Solutions Laboratory is looking for a Clinical Research Scientist to join our Assay Development team. In this position, you will be responsible for development, implementation, and improvement of novel clinical assays using a wide range of methodologies and testing platforms. Successful candidates should have experience with molecular biology techniques, such as nucleic acid extraction, qPCR, primer/probe design, NGS, and microarray, in addition to experience with ELISAs at a minimum. Candidates should also have excellent communication skills including written and oral data presentations. A record of accomplishment in both troubleshooting and assay/technique development is preferred. Candidates must possess the ability to progress multiple projects simultaneously.
Responsibilities:
· Independently design and execute experimental plans for development and validation of clinically applicable assays.
· Assist with conceptualization and theoretical development of novel assays with clinical application.
· Analyze, interpret, and present experimental data and results.
· Generate accurate validation reports and standard operating procedures for use in a clinical production laboratory.
· Assist with implementation, training, troubleshooting and improvements of developed clinical assays.
· Work with QC/QA department to implement required quality assurance protocols for new and existing production assays.
Qualifications:
· Master's or PhD in biology with a research focus in molecular biology is required.
· Previous clinical experience with assay development or troubleshooting is required.
· Demonstrated experience with qPCR, NGS, and ELISAs required. Additional experience with flow cytometry, microarray, laboratory automation is highly preferred.
· Demonstrated ability to work independently on multiple projects simultaneously with minimal supervision is required. Demonstrated ability to assist junior members of the team on additional projects is highly preferred.
Job Type: Full-time Salary Monday-Friday with some weekend work required.
Application Questions:
· How many years of clinical research experience in molecular biology do you have?
o Must have 2 years of post-academic experience
· What is your highest level of completed education?
o Must have PhD
· Are you currently local to Alpharetta GA?
o Must be local
· Are you authorized to work in the United States?
Must be authorized to work in the US without sponsorship
Job Type: Full-time
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Work Location: In person
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