YOUR FREELANCE PROJECT

The ARISTO Group supports you in your search for the best projects that are currently available on the market. Through direct contact with decision-makers, we offer you access to exceptional positions and thus give you a competitive advantage.

  • Complete independence
  • Free action in terms of orders and salaries
  • No fixed salary limits
  • Opportunity to claim everyday things for tax

CURRENT OFFERS
FREELANCE

Senior Produkt Manager (m/w/d)

  • OTC-Produktmanagement
  • natürliche Arzneimittel
  • Mittelstand

Koblenz

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Clinical Research Associate (m/w/d)

  • Klinischer Monitor
  • Pharma
  • CRO

Karlsruhe

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Clinical Research Associate (m/w/d)

  • Klinisches Monitoring
  • Pharma
  • CRO

Stuttgart

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Clinical Research Associate (m/w/d)

  • Klinischer Monitor
  • Pharma
  • CRO

Bonn

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OUR RECRUITING PROCESS
FOR CANDIDATES

Aristo is characterized by the 360 ° model.
You will be supported comprehensively and sustainably by one contact person throughout the entire process.

This form of placement guarantees you high quality standards and access to highly specialized projects and positions.

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1.CANDIDATE QUALIFICATION

2.PRESENTATION OF THE HOLIDAY

3.VORSTELLUNG IHRES PROFILS PRESENTING YOUR PROFILE

4.INTERVIEW - PROCESS

5.CONTRACT PROCESSING

6.SUSTAINABLE SUPPORT



BENEFITS MIT ARISTO

  • 01Many years of specialist know-how
  • 02Advice comes before sales
  • 03Fast & efficient way of working
  • 04Open communication
  • 05Absolute discretion & confidentiality

WE PROMOTE YOUR CAREER

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LATEST INFORMATIONFOR CANDIDATES

Die Veröffentlichung der Medizinprodukteverordnung (Medical Device Regulation) – Sie ist da… (Teil 2)
Große Neuerungen erfordern eine große Reaktion. 175 Seiten lang unterteilt in 10 Kapitel – lesen Sie hier den zweiten Teil unserer Blogreihe zur Veröffentlichung der neuen "Medical Device Regulation"!
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Die Veröffentlichung der Medizinprodukteverordnung (Medical Device Regulation) – Sie ist da… (Teil 1)
175 Seiten lang, unterteilt in 10 Kapitel - Lesen Sie den ersten Teil unseres zweiteiligen Berichts über die wichtigsten Neuerungen in der neuesten Veröffentlichung der "Medical Device Regulation"!
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