Job Description

CRA in Munich, Bayern

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Location

Munich, Bayern

Salary

Negotiable

Contract

Contract

Are you an experienced Clinical Research Associate with considerable clinical research monitoring experience? Are you based in Germany and looking for a new contract role? If so, we are keen to hear from you!

Our leading CRO client is recruiting for a CRA to be based in Germany, performing and coordinating all aspects of the clinical monitoring and site management process.

This position is offered on a 12 month contract basis initially, working 32 hours per week.

Description:

  • Work in accordance with ICH Good Clinical Practices, FDA guidelines, local regulations and PPD Standard Operating Procedures
  • Conducts site visits to assess protocol and regulatory compliance and manages required documentation.
  • Responsible for ensuring that data will pass international quality assurance audits.
  • Represent our client in the global medical research community and develops and maintains collaborative relationships with investigational sites and client company personnel.
  • Will assist project manager or clinical team manager on assigned projects and will take a lead role where required.
  • Will support the line manager to mentor, train and contribute to the development of junior clinical team members.
  • Required to travel 60-80% on average.

Education and Experience:

  • Degree in a science related field or, a certified health care professional, or equivalent certification/licensure from an appropriately accredited institution.
  • Considerable clinical research monitoring experience with a demonstrated high level of expertise in all aspects of clinical monitoring.
  • Expert clinical monitoring skills.
  • Expert knowledge of FDA guidelines, GCPs and applicable Standard Operating Procedures.
  • Skills to mentor and train other monitors in a positive and effective manner.
  • Demonstrated ability to evaluate medical research data and proficient knowledge of medical terminology.
  • Proven flexibility and adaptability.
  • Excellent team player with team building skills.
  • Effective presentation skills.
  • Ability to work independently as required.
  • Ability to utilize problem-solving techniques applicable to constantly changing environment.
  • Fluency in English and in the country's native language.
  • Valid Driver's License.

Disclaimer

This vacancy is being advertised by either Advanced Resource Managers Limited, Advanced Resource Managers IT Limited or Advanced Resource Managers Engineering Limited ("ARM"). ARM is a specialist talent acquisition and management consultancy. We provide technical contingency recruitment and a portfolio of more complex resource solutions. Our specialist recruitment divisions cover the entire technical arena, including some of the most economically and strategically important industries in the UK and the world today. We will never send your CV without your permission. Where the role is marked as Outside IR35 in the advertisement this is subject to receipt of a final Status Determination Statement from the end Client and may be subject to change.

Job reference 128472_1763564214
Date posted 19 November 2025
Sector Life Sciences

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Ruby Willard

Ruby Willard

Principal Consultant

+44 (0)2392 228203

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