
Molecular Biologist
4 weeks ago
The ideal candidate will bring deep technical expertise in q PCR assay development, optimization, and data analysis, specifically aligned with preclinical drug screening and mechanistic in-vitro studies.
This is a strategic consulting role aimed at enhancing our molecular biology capabilities in gene expression, target validation, and biomarker discovery.
Key Responsibilities: Provide technical leadership in the design, development, and validation of q PCR assays for in-vitro studies including cytotoxicity, gene expression profiling, and pathway analysis.
Advise on sample preparation, RNA/DNA extraction, and quality control specific to in-vitro systems.
Guide the team in primer/probe design, assay optimization, and standard curve generation.
Troubleshoot experimental issues and recommend improvements to protocols and workflows.
Ensure robust data integrity, statistical soundness, and scientific documentation of q PCR results.
Review experimental designs to align with regulatory and scientific requirements for GLP-compliant preclinical studies.
Train lab scientists on best practices for q PCR technique and data interpretation.
Collaborate with research scientists and study directors to integrate molecular endpoints in preclinical study design.
Stay updated with emerging trends, technologies, and best practices in molecular biology and q PCR.
Qualifications: Ph.
D.
or Master's in Molecular Biology, Cell Biology, Biotechnology, or a related field.
Minimum 10 years of hands-on experience in molecular biology techniques, with a strong focus on q PCR in preclinical models.
Excellent analytical, documentation, and communication skills.
Desirable Skills: Knowledge of cell-based assay systems, molecular endpoints, and biomarker quantification.
Exposure to RT-q PCR, mi RNA analysis, or multiplex PCR.
Engagement Type & Compensation: Consulting basis – Part-time, Remote, Hybrid Remuneration commensurate with experience and scope of involvement.
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