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Central Lab Scientist – Clinical Laboratory

 

Central Lab Scientist – Clinical Laboratory

Laboratory         ·        Singapore – Singapore       ·       Full time

 

Job Summary

Our clinical laboratory activities are growing rapidly, and we are currently looking to add a Scientist to out team. As a Scientist, you will act as a leader in this respective area and will participate in and direct research and development within the laboratory. You will aid in the development and growth of the clinical laboratory department and will oversee the implementation of new technologies and instrument platforms in the lab. 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 medically-reliable data are being generated;
  • Interact with corporate leadership, 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; 
  • Ability to troubleshoot technical issues;
  • Ability to meet aggressive timelines;
  • Oversee the design, validation and maintenance of analytical methods in clinical trial environments;
  • Oversee the analysis of laboratory testing; and
  • Oversee technical areas (i.e., Clinical Chemistry/Hematology/Coagulation).

 

Qualifications

  • PhD in Laboratory Medicine, Immunology, Clinical Chemistry, Clinical Pathology or other similar area;
  • Experience in automation of data analysis is considered a plus;
  • Excellent project management and communication skills;
  • Proficiency in English is required;
  • Experience in a Central Laboratory setting or with clinical research preferred;
  • Candidates with experience in ELISA, clinical chemistry or genomics are welcome to apply as well.

 

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
  • 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

 

What to Expect Next:

A member of our recruitment team will review your qualifications and, if interested, you will be contacted for an interview.

 

EO/AA Employer M/F/Disability/Vets

 

Please click here to apply.

 

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