Central Lab Scientist - Molecular

Medpace; Singapore; On-site; SGD 60,000 - 80,000; Full time

Job summary

A clinical research organization is seeking a Scientist to lead laboratory operations in Singapore. The role involves overseeing molecular method validations and participating in research and development. Candidates should hold a PhD and have experience in molecular assay design and data analysis, particularly in qPCR and sequencing. Strong critical thinking and interpersonal skills are essential for this full-time, office-based position.

Benefits

Flexible work environment

Competitive compensation and benefits

Career growth opportunities

Employee health and wellness initiatives

Qualifications

• 2-3 years of experience in molecular assay design and development.
• Experience with analysis of qPCR data is required.
• Excellent record-keeping skills are mandatory.

Responsibilities

• Monitor laboratory operations for data accuracy and reliability.
• Participate in meetings with sponsors and project management.
• Troubleshoot technical issues related to sequencing.

Skills

Critical thinking

Problem-solving

Interpersonal skills

Education

PhD in Laboratory Medicine or related field

Tools

qPCR

Sanger sequencing

Next Generation Sequencing

Job description

Job Summary

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 timelines
• Develop 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 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?

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 package
• Competitive PTO packages
• Structured career paths with opportunities for professional growth
• Company-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 2024
• Continually 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.