Clinical Project Administrator

Job Location(s) DE-Munich
Job Number
Job Category
Clinical Operations
Position Type

Job Overview

As an integral part of everything we do, our employees make a difference in the lives of millions of people… and you will too.


If you want to start or develop your career in Clinical Trials and you are thinking about long term opportunities we are happy to invite you to apply to one of the biggest Clinical Research Organizations around the world. We are a global leading CRO and have helped the pharmaceutical industry develop more medicines worldwide than any other company, including the top 50 best-selling drugs on the market.


Explore our Clinical Project Administrator profile and apply now!


We have Clinical Project Administrator job available to work directly with large Pharmaceutical companies in cutting edge areas like Oncology, Cardiology or Diabetes.


You will provide support to CRAs and CTLs with: essential document collection, Site Initiation Visits, amendments... Your trained-eye will be vital to perform study documents QC review for archiving (paper and eTMF). You will set up and maintain investigator files, personalize contracts for sites. You will also be involved in payments and contracts.

We are looking for professionals with strong interest in Clinical Trials. We do require BA degree but it does not need to be in life sciences. Additional requirement is having good English language skills and having no problems with discussing complex matters with German speaking professionals.


We offer:

  • Work environment where your job is appreciated
  • Friendly colleagues ready to help you
  • Flexible working hours
  • A package of benefits

Sounds interesting? Feel free to apply directly via career portal or get in touch with our recruiter, Krzysztof Orzechowski available on linkedin or at

Education / Qualifications

- University degree 


We expect from you: 

- Previous experience in the field (around one year)
- Degree educated.
- Fluency in German and English language.
- Understanding of the clinical trial process;
- Good oral and written communication skills
- Ability to set priorities and handle multiple tasks simultaneously

At Covance, you will join like-minded professionals who, together, build our reputation as one of the world's largest and most respected contract research organizations. In choosing Covance, you will be part of a dedicated team that makes a difference in helping to deliver life-saving and life-enhancing medicines to people around the world. We have vocations in different areas of Russia.

We welcome your application and believe this decision may be the most rewarding career move you will ever make



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