Posted: 5 January 2022

Consultant Non-Clinical Development – 3D-PharmXchange

Location: Tilburg, The Netherlands
Hours: 40

Company profile

3D-PharmXchange is a Dutch Life Sciences consultancy and operational support firm located in Tilburg and Oss. We are dedicated to the development of (bio-)pharmaceuticals and diagnostics.
Our team of experts covers the key areas of pre-clinical, clinical, CMC, regulatory affairs and project management. In addition, we provide out-licensing and interim management support. Our clients are leading big pharma companies as well as innovative biotech start-ups.

Job description

For the various projects that we are running for our clients, we are looking for a consultant non-clinical development to join our team of consultants. The ideal candidate has a background in ADME (preferred) and Toxicology and is able to look beyond his or her borders and has the ambition to grow in a young and growing organization. Training and/or coaching will be provided in specific
areas if needed.

Minimal requirements

  • PhD or equivalent, or MSc degree in Life Sciences, with experience in drug development or
    similar field
  • At least 3 years of experience as an ADME study director, non-clinical project manager or other drug development role
  • Communication skills: good oral, writing and presentation skills
  • Personality skills: pro-active, team player, results-oriented, can-do mentality and ability to put yourself in the position of our clients
  • Experience in a number of the following areas and roles (not all required):
  • Experience in conducting or monitoring drug metabolism studies
  • Experience in designing, monitoring or conducting safety (toxicology) studies at CRO’s and analyzing/presenting data
  • Knowledge of and experience in global regulatory requirements for the development and registration of new medicinal products (chemical entities and/or biologicals)
  • Experience in drafting and reviewing biocompatibility and/or safety assessments, researching literature and toxicology database resources, and summarizing information
  • Experience in writing and/or reviewing documents for specific global regulatory purposes, e.g. investigators’ brochures, IMPD, (non-)clinical dossier (eCTD), etc.
  • Understanding of Good Laboratory Practice (GLP) regulations
  • Project coordination and project team participation

A Great Team & Atmosphere

We offer a challenging job in an international environment, working for top entrepreneurs and big pharma. You will be working in a very dynamic, young, and growing team and have the freedom to shape your work. Although 3D-PharmXchange is well-known as an experienced partner in drug development, this doesn’t mean it is all about business. Our main aim is to centralize and empower our consultants. Not only professionally but also informally.

For more information about this vacancy, please contact Managing Partner +316 28209882

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