CheckMark Labrecruitment

Gepubliceerd: 17 days ago

Scientist Clinical Immunology

Regio Leiden
Gepubliceerd: 17 days ago
Solliciteer nu
Waar ga je aan de slag - Where will you work

A international pharmaceutical company. This department is responsible for the immunological evaluation of vaccine candidates in clinical trials.


Wat ga je doen - What will your job be

You will garantee the correct design and execution of experiments for the development, qualification and validation of immunological assays to be used in the analysis of samples from clinical trials. Are you an expert in immunology? Apply now!

As Scientist Clinical Immunology you will garantee the correct design and execution of experiments for the development, qualification and validation of immunological assays to be used in the analysis of samples from clinical trials. To do so, you:

  • Perform experiments on a regular basis to support assay development and maintain your technical edge by following relevant literature and knowledge in the field
  • Generate high-quality scientific reports to document your work
  • Are responsible for the long-term life cycle management of the methods, together with the key reagents, equipment and data analysis tools required for the assay to be performed
  • Your activities must be executed, documented and reported according to Good Clinical Laboratory Practice (GCLP) quality requirements
  • Furthermore, you are responsible for instructing associate and assistant scientist on the scientific fundamentals of the assays, and you will critically review the data generated by them

Wat vragen wij - What are we looking for

For the position of Scientist Clinical Immunology we are looking for a candidate with at least 2 years of experience in industry, highly preferably within a pharmaceutical, biotech company

  • MSc or PhD (preferred) in biological/medical sciences or equivalent, with strong immunology or virology background
  • Hands-on experience in the development to validation of serology or cell based assays (ELISA, Virus Neutralization Assays, ELISPOT, Flow cytometry or similar) according to regulatory standards (e.g. ICH)
  • Experience in high-throughput assays is desirable
  • Knowledge of biostatistics, experience in statistical programs such as SPSS or JMP is a must
  • Experienced in working under quality standards such as GCLP, GCP or GMP is a plus
  • Excellent communication, coordinating and planning skills
  • As a person you are quality minded, flexible and you remain calm and positive under pressure. Furthermore you are a team player who is able to motivate others

Wat hebben we te bieden - What do we offer
  • Secondment via CheckMark Labrecruitment for 1 year (longer term anticipated)
  • Salary indication starting from €4200,- based on fulltime
  • Fulltime position (40 hours/week), 32 hours is discussable for candidates with relevant work experience
  • Working one day from home is discussable

Wil je meer weten - More information

Neem voor meer informatie contact op met Jurjen Wilschut: 0182 590 212
Vacaturenummer: 6618

Solliciteer nu