Clinical Drug & Ancillary Supplies Specialist ()


Position : Clinical Drug (and Ancillary) Supplies Specialist or Associate

Location : Brussels office-based

You can make a difference by helping to deliver life-saving and life-enhancing medicines to people around the world.

Covance is one of the world’s most dynamic drug development services companies, providing integrated, tailored solutions to the pharmaceutical and biotechnological industries.
We are currently looking for a

Drug (and Ancillary) Supplies Specialist

About the job

  • Support the delivery of Clinical (drug) and Ancillary (material) supplies component of international studies (planning, management and maintenance).
  • Manage the drug/ancillary supplies vendor.
  • Act as contact with project team during clinical and ancillary start-up activities for global studies.
  • Perform and coordinate label development, review and country translations according to set procedures and regulatory requirements.
  • Where appropriate be the key contact for importation logistics and document exchange to ensure smooth clinical supply transportation arrangements are agreed and set up.
  • Provide consultancy with regard to clinical & ancillary supply distribution strategy for global studies.
  • Work closely with drug and ancillary supply distribution, IVRS/IRT and label translation vendors during the set up and maintenance of the project.

About you

  • University/College degree (life science preferred), or certification in a related allied health profession (e.g., nursing certification, medical or laboratory technology)
  • 3 years work experience in clinical research, including a strong working knowledge of the ICH-GCP guidelines and FDA, GMP regulations.
  • Ideally 3 years relevant clinical research experience in a pharmaceutical company/CRO, including at least 1 year of clinical and ancillary supplies management responsibility. Nonetheless, we will also be looking at starter profiles with scientific background (Associate level).
  • Working knowledge of ICH, FDA, GMP and other applicable regulations/guidelines; familiarity with clinical supply related documents.
  • Strong networking abilities and an ability/willingness to work with internal and external stakeholders across the globe
  • Good organizational, time management, communication and computer skills
  • Excellent English

Don´t assume all companies will bring you the same!

Job titles may be similar, but the content of your work day is what counts. So think for a second on the working environment of a company capable of contributing to the development of:

  • 50% of the latest breakthrough oncology treatments
  • The top 25 currently marketed medicines

And being ranked the 4th World’s Most Admired Health Care Pharmacy Company in 2012.

As we are a truly global, we can offer you international career development.

As we are a full-service CRO, our structure allows the development of a varied career, touching different angles of the Drug Development Process in the same company.

And we proud ourselves to have a team of dedicated managers, who will be at your side to make the most of your career with us.

How to apply

To learn more and apply please follow the link:

Employer Covance is committed to diversity in the workplace and is an equal opportunity employer. (M/F/D/V). Your confidentiality and privacy are important to us.



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