Posted to MedZilla on 8/20/2017


Germany, Freelance CTA - Munich - Global pharma CR_TS_13021-MZ


An exciting opportunity for a Project Assistant has opened up at an international contract research organisation providing drug discovery, lifecycle management and laboratory services. With offices in over 45 countries and approximately 13,000 professionals, this company provide innovative ideas behind multiple sectors. This particular position will be based in Munich.

Job Overview:

This is a great opportunity for CTA's/Project Assistants at any level currently working within the life science sector for pharmaceutical companies, Biotech companies or Clinical Research Organizations (CRO) who would enjoy the opportunity to work for a CRO dedicated to one client.

As the trusted partner of some of the most innovative big pharma and biotech companies; our PA's have the opportunity to work on challenging projects across a wide range of therapy areas. Our vision is to be the global leader in our industry; based on consistent quality and execution, exceptional customer-aligned service and constant innovation.

You should thrive in project teams and be focused on delivering exemplary levels of customer service. You will have excellent communication and organisational skills and a self-motivated, flexible, and professional attitude. You must be able to prioritise and work well within a multi-national team environment and have an in-depth knowledge of Microsoft Word, Excel and preferably PowerPoint. You will have a good standard of education and extensive administration experience.

In return, we will offer you a positive and supportive working environment within one of the most engaged teams in the industry; who are truly recognised as the cornerstone of our success. We will provide you with meaningful work and the opportunity to acquire valuable personal and professional skills.

Education and Experience:

  • Bachelor's Degree or good general education with secretarial qualification preferred or equivalent combination of education, training and experience that provides the individual with the required knowledge, skills, and abilities.
  • General administration experience. Clinical research administration experience preferred.
  • Self-motivated, positive attitude with good oral and written communication and good interpersonal skills.
  • Ability to work in a team or independently as required.
  • Good organizational skills and strong attention to detail, with ability to handle multiple tasks efficiently and effectively.
  • Ability to effectively analyse and update project specific data/systems to ensure accuracy and efficiency.
  • Flexibility and adaptability to reprioritize workload and provide efficient support to meet changing project timelines.
  • Customer focus.
  • Ability to attain and maintain a working knowledge of applicable ICH GCP, FDA guidelines, local regulations, client SOPs and WPDs.
  • Good English language and grammar skills.
  • Good computer skills, proficient in MS office and able to obtain and retain knowledge, so as to maintain and update computer based clinical trial database systems.

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.
In case you have difficulty in applying or if you have any questions, please call Theodora Savlovschi-Wicks on +44 203 7520 314 or upload your CV on our website -
A full job description is available on request.
ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

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