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Scientist: Diagnostic Development
Up to US$35 per hour + Highly Competitive Salary
- Contract
- Biological Sciences, Medicinal Chemistry, Pharmacology
- United States
New Haven, USA
Posting date:
19 Jan 2024
SC.SB.58071
This vacancy has now expired. Please see similar roles below...
Scientist: Diagnostics Development - Contract - Onsite
Proclinical is seeking a Scientist: Diagnostic Development to join a global biopharmaceutical company. This is a contract role located in New Haven, CT.
Skills & Requirements:
- Ph.D. in life sciences, physical sciences, bioengineering or related field with 2+ years of biotech, biopharmaceutical or academic R&D experience in assay, platform and technology development
- Experience in developing and optimizing biomarker assays and diagnostic tests, including but not limited to immunoassays (ELISA, Luminex, Quanterix), molecular assays (qPCR, isothermal, nucleic acid hybridization) or cell-based assays (Microscopy, FACS)
- Experience in upstream sample processing techniques (tissue, cultured cells, biological fluids such as whole blood, plasma, serum, urine etc.)
- Experience in bioconjugation, microbead chemistry, ligand binding assay and related nanobiotechnology
- Working knowledge in traditional and advanced biomarker and diagnostic methodologies, platforms, technologies and techniques
- Working knowledge in fluorescence, luminescence and electrochemical measurements
- Knowledge in diagnostic test development, from biomarker development to regulatory approval
- Knowledge in medical device development
- Must be eligible to work in the US.
The Scientist: Diagnostics Development will:
- Designing and executing proof-of concept experiments to support multiple programs
- Developing and optimizing bioassays and tests
- Independently analyzing experimental data, performing literature reviews, proposing and executing experiments to support diagnostic development timelines and decisions
- Solving difficult complex problems using innovative and practical ideas and workflows
- Developing and authoring lab SOPs and protocols
- Adopting or developing new technologies, methodologies and platforms to improve or expand current testing capabilities
- Working closely and managing projects with contract research organizations (CROs)
- Cultivating a collaborative environment with experts from cross-functional teams
- Maintaining high standards of professional accountability, quality, and compliance
If you are having difficulty in applying or if you have any questions, please contact Shannon Briggs at (+1) 215-531-6914 or s.briggs@proclinical.com.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Proclinical Staffing is an equal opportunity employer.
INDSCIC