Senior Scientist: Genomics
About The Position
Join Us as a Senior Scientist – Make an Impact at the Forefront of Innovation. We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years. The clinical genomics research scientist is responsible for helping to development clinical genomic workflows and perform genomic and genetic testing of clinical trial biospecimens to advance translational research initiatives. This includes but is not limited to responsibilities for genomics and gene expression profiling (GEP) biomarker assay technology/ platform selection, evaluation of in-house or vendor choice per assay use requirements, development, optimization, qualification/validation and execution of biomarker analysis for translational medicine and clinical programs. Successful candidates must have a strong technical background in genomics and transcriptomics and its application in clinical programs, additional specific requirements listed below.
Requirements
- Bachelor's degree or equivalent and relevant formal academic / vocational qualification
- Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 4-6 years). In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
- Prior experience working in a CLIA-licensed lab is a plus.
- Must be capable of working and operating in a laboratory environment for the entirety of the work schedule.
- Experience with NGS or GEP applications is required.
- Demonstrated experience in assay development for genomics assets, preferably in a pharma, biotech, diagnostic, or clinical lab setting.
- Hands -on experience with genomics platforms (NGS, qPCR, variant analysis) for assay development, qualification/validation, troubleshooting, and reviewing run QC data.
- Understanding of fit-for-purpose genomics assay validation principles for clinical assays.
- Knowledge of clinical sample analysis regulatory and quality frameworks (e.g., GCP, CLIA, CAP, NYDOH) is a plus.
Responsibilities
- Assist in planning and executing genomics and transcriptomics experiments in the lab
- Perform hands-on lab work on-site, supporting the development and optimization of biomarker assays
- Help design and run genomic tests, including gene expression and biomarker profiling assays
- Support assay development, testing, and validation following established protocols and SOPs
- Assist in collecting, organizing, and analyzing experimental data
- Help prepare reports, lab protocols, and summaries of experimental findings
- Support coordination with external vendors and internal teams as needed
- Maintain accurate lab records and documentation in compliance with best practices
- Collaborate with cross-functional teams, including data analysis, sample management, and clinical operations
- Stay current with emerging genomics technologies and contribute to their evaluation
- Follow lab best practices and contribute to continuous process improvement
- Support and learn from senior scientists and team leads in a mentorship environment
Benefits
- A choice of national medical and dental plans, and a national vision plan, including health incentive programs
- Employee assistance and family support programs, including commuter benefits and tuition reimbursement
- At least 120 hours paid time off (PTO)
- 10 paid holidays annually
- Paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave)
- Accident and life insurance
- Short- and long-term disability in accordance with company policy
- Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan
- Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount
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What This Job Offers
Job Type
Full-time
Career Level
Senior
