Molecular Scientist
il y a 2 semaines
Job Summary:
Responsibilities:
- Monitor laboratory operations in order to verify that accurate, precise, and reliable data are being generated for clinical trials;
- Interact with corporate leadership, scientific liaison, project management, administration, government agencies, accrediting agencies, and potential sponsors/clients to gain information and knowledge required to make appropriate business and/or operational recommendations and decisions;
- Participate in general capabilities and bid defense meetings with sponsor;
- Ability to troubleshoot technical issues related to quantitate PCR, Sanger sequencing and Next Generation Sequencing (NGS) runs and subsequent data analysis;
- Ability to meet aggressive timelines (e.g., validation, database lock etc.);
- Routine molecular data analysis, review, and approval of clinical reports with specific timelines;
- Develop and conduct training within molecular genomics;
- Maintaining instrument compliance with 21 CFR Part 11;
- Review and write Validation Plans/Reports/SOPs;
Qualifications:
- PhD in Laboratory Medicine, Molecular Biology, Biochemistry/Biotechnology, Clinical Pathology or other similar area;
- 2-3 years of experience in molecular assay design, assay development in a clinical diagnostics environment or a translational research laboratory.
- Experience with analysis of qPCR, Sanger sequencing and NGS data is required;
- Strong knowledge of viral load and viral shedding is preferred.
- Excellent record keeping and organization skills are required;
- Analytical Method Validation experience is preferred;
- Previous experience in a central lab environment is preferred;
- Experience with human samples is preferred.
- Excellent interpersonal skills to effectively interact with and influence stakeholders, both internally and externally, are required.
- Excellent capacity to work in a team setting is required.
Medpace Overview:
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.
Why Medpace?:
When you join Medpace, you become part of a team dedicated to supporting the development of ground-breaking drugs and devices. Our employees provide hope for those living with debilitating diseases. We invite you to be a part of something that is impacting millions of people around the globe while enjoying a competitive total compensation and benefits package and internal growth opportunities.
**Awards**:
- Medpace historically named a Top Cincinnati Workplace by the Cincinnati Enquirer
- Recognized by Forbes as one of America's Best Mid-size Companies in 2021
- Medpace ranks amongst top CROs for site ratings across all 10 important attributes including CRA training, preparation & organization, accessibility of staff, open communication, and ensuring timely drug availability
- Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
- Ranked in the top 10 on the 2021 LinkedIn Top Companies list in Cincinnati
**What to Expect Next**:
A member of our recruitment team will review your qualifications and, if interested, you will be contacted for an interview.
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