Our clinical laboratory activities are growing rapidly, and we are currently looking to add to our scientific team. The Scientist will act as a leader in the department and will participate in and direct research and development within the laboratory. S/he will aid in the development and growth of the molecular area and will oversee the daily operations and molecular method validations. The ideal candidate will have strong critical thinking and problem-solving abilities. This position will be a full-time, office-based position in Singapore.
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 quantitative PCR and Sanger sequencing. Ability to understand Next Generation Sequencing (NGS) workflows and procedures; be able to communicate with Bioinformatics data analysis scientists on NGS quality issues.Ability to meet aggressive timelines (e.g., validation, database lock etc.);Routine molecular data analysis, review, and approval of clinical reports with aggressive timelinesDevelop and conduct training within molecular genomics;Maintaining instrument compliance with 21 CFR Part 11;Review and write Validation Plans/Reports/SOPs and; 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 data is required. Analysis of Sanger sequencing and NGS data is very desirable;Excellent record keeping 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. Medpace OverviewMedpace 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?People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.
The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.
Medpace Perks
Flexible work environment Competitive compensation and benefits packageCompetitive PTO packagesStructured career paths with opportunities for professional growthCompany-sponsored employee appreciation events Employee health and wellness initiatives
Awards
Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
What to Expect Next
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
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