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Medpace

Global CRO delivering full-service clinical trials

Medical Technologist - Chemistry

Diagnostics & Laboratory ProfessionalsConfirmed live in the last 24 hours
Full-timeLeuven, BelgiumNo salary listed

About the Job

Requirements

  • A Bachelor of Science degree in Biomedical Laboratory Technology, option Medical Laboratory Technology, and certification by the national-level professional evaluation organization are required.
  • Basic knowledge of drug therapy techniques and medical terminology is required.
  • Experience working with chemistry is required.
  • Excellent written and verbal communication skills and a good command of written and spoken English are required.
  • Ability to work in a team environment, work independently, and demonstrate effective interpersonal skills is required.
  • A professional demeanor, strong work ethic, sense of responsibility, studiousness, accuracy, and a solution-minded approach are required.
  • Ability to handle stress effectively is required.

Responsibilities

  • Perform low-, moderate-, and high-complexity testing according to applicable Standard Operating Procedures.
  • Train on different sets of automated instrumentation and learn maintenance and troubleshooting skills.
  • Perform quality control procedures, evaluate and interpret quality control data, and implement and document corrective action as needed.
  • Perform documentation and routine laboratory system operations.
  • Work alongside Medical Laboratory Scientists and PhD Scientists to develop and validate new tests and methods for routine and biomarker testing.
  • Keep track of inventory.
  • Adhere strictly to safety procedures.
  • Work a rotation schedule of Monday through Friday and Tuesday through Saturday.

Desired Qualifications

  • Previous experience in a haematology area is a plus.

About the Company

Medpace

Global CRO delivering full-service clinical trials

Medpace is a global Contract Research Organization that provides end-to-end clinical development services for pharmaceutical, biotechnology, and medical device companies. It manages Phase I–IV trials from study design and regulatory submissions to monitoring, data management, biostatistics, and final reporting, using a single integrated team. A key differentiator is its ownership of integrated laboratories—global central labs, a bioanalytical lab, and imaging/ECG core labs—ensuring streamlined workflows and consistent data. Its physician-led, scientifically driven approach and single-vendor model aim to reduce sponsor oversight and help bring therapies to market efficiently, with operations in over 40 countries.

Company size
5,001-10,000
Company stage
IPO
Headquarters
Cincinnati, OH
Founded
1992

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