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Clinical Research Associate (CRA)

Eurofins

Clinical Research Associate (CRA)

full-timePosted: Jan 16, 2026

Job Description

Description

The main task of the CRA is to act as a link between sponsor, CRO and trial site as well as to perform quality control of clinical trials. The focus is on clinical studies conducted in-house at bioskin or in the Northern German region.

 

Your main responsibilities: 

  • Perform all kind of the monitoring visits (site selection, initiation, periodic and close-out visits) as well as remote monitoring
  • Generation and updating of monitoring plans and site initiation presentation
  • Evaluating the quality and integrity of site practices
  • Act as contact for clinical trial suppliers and other vendors as assigned
  • Identifying and escalating protocol deviations, discrepancies in data, and non-compliance to clinical trial protocols
  • Close cooperation with the different departments in-house at bioskin as well as freelance CRAs
  • Compliance with protocol, GCP/ICH Guidelines

Qualifications

The ideal Candidate will need the following experience to be considered:

  • Min. 2 years of the clinical monitoring experience (preferred Dermatology)
  • Degree in a scientific or medical discipline or equivalent
  • Very good knowledge of Good Clinical Practice/ICH Guidelines
  • Proven ability to work independently in a fast-paced environment
  • Excellent communication, interpersonal, and organizational skills
  • Fluency in German and a high level of English language
  • located in Hamburg

Additional Info

Contacts by headhunters, recruiting or staffing agencies are not accepted!

Company Description

Eurofins bioskin is a leading niche CRO with unique understanding and capabilities for both early and late phase development of dermatological and related products. Since its inception in 1992, eurofins bioskin has been recognized as a valuable partner for dermatological product development. Starting as a small Contract Research Organization (CRO) specialized in conducting early phase safety and efficacy trials, eurofins bioskin has grown into a full-service CRO offering global dermatologic consulting and regulatory services and all services for management of Phase I-IV drug trials and claim support/safety studies. eurofins bioskin is headquartered in Hamburg, Germany.

Locations

  • Hamburg, HH, Germany (Remote)

Salary

Estimated Salary Rangemedium confidence

60,000 - 100,000 EUR / yearly

Source: ai estimated

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • Monitoring de sites cliniquesintermediate
  • Connaissances GCP/ICHintermediate
  • Gestion de protocoles cliniquesintermediate
  • Communication interpersonnelleintermediate
  • Travail indépendantintermediate

Required Qualifications

  • 2+ ans d'expérience en monitoring clinique (préféré dermatologie) (experience)
  • Diplôme scientifique ou médical (experience)
  • Excellente connaissance GCP/ICH (experience)
  • Allemand et anglais fluent (experience)
  • Localisé à Hamburg (experience)

Responsibilities

  • Effectuer visites de monitoring (sélection, initiation, périodiques, close-out)
  • Générer et updater plans de monitoring
  • Évaluer qualité des pratiques des sites
  • Identifier et escalader déviations de protocole
  • Coopérer avec départements internes et CRAs freelance

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Eurofins logo

Clinical Research Associate (CRA)

Eurofins

Clinical Research Associate (CRA)

full-timePosted: Jan 16, 2026

Job Description

Description

The main task of the CRA is to act as a link between sponsor, CRO and trial site as well as to perform quality control of clinical trials. The focus is on clinical studies conducted in-house at bioskin or in the Northern German region.

 

Your main responsibilities: 

  • Perform all kind of the monitoring visits (site selection, initiation, periodic and close-out visits) as well as remote monitoring
  • Generation and updating of monitoring plans and site initiation presentation
  • Evaluating the quality and integrity of site practices
  • Act as contact for clinical trial suppliers and other vendors as assigned
  • Identifying and escalating protocol deviations, discrepancies in data, and non-compliance to clinical trial protocols
  • Close cooperation with the different departments in-house at bioskin as well as freelance CRAs
  • Compliance with protocol, GCP/ICH Guidelines

Qualifications

The ideal Candidate will need the following experience to be considered:

  • Min. 2 years of the clinical monitoring experience (preferred Dermatology)
  • Degree in a scientific or medical discipline or equivalent
  • Very good knowledge of Good Clinical Practice/ICH Guidelines
  • Proven ability to work independently in a fast-paced environment
  • Excellent communication, interpersonal, and organizational skills
  • Fluency in German and a high level of English language
  • located in Hamburg

Additional Info

Contacts by headhunters, recruiting or staffing agencies are not accepted!

Company Description

Eurofins bioskin is a leading niche CRO with unique understanding and capabilities for both early and late phase development of dermatological and related products. Since its inception in 1992, eurofins bioskin has been recognized as a valuable partner for dermatological product development. Starting as a small Contract Research Organization (CRO) specialized in conducting early phase safety and efficacy trials, eurofins bioskin has grown into a full-service CRO offering global dermatologic consulting and regulatory services and all services for management of Phase I-IV drug trials and claim support/safety studies. eurofins bioskin is headquartered in Hamburg, Germany.

Locations

  • Hamburg, HH, Germany (Remote)

Salary

Estimated Salary Rangemedium confidence

60,000 - 100,000 EUR / yearly

Source: ai estimated

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • Monitoring de sites cliniquesintermediate
  • Connaissances GCP/ICHintermediate
  • Gestion de protocoles cliniquesintermediate
  • Communication interpersonnelleintermediate
  • Travail indépendantintermediate

Required Qualifications

  • 2+ ans d'expérience en monitoring clinique (préféré dermatologie) (experience)
  • Diplôme scientifique ou médical (experience)
  • Excellente connaissance GCP/ICH (experience)
  • Allemand et anglais fluent (experience)
  • Localisé à Hamburg (experience)

Responsibilities

  • Effectuer visites de monitoring (sélection, initiation, périodiques, close-out)
  • Générer et updater plans de monitoring
  • Évaluer qualité des pratiques des sites
  • Identifier et escalader déviations de protocole
  • Coopérer avec départements internes et CRAs freelance

Target Your Resume for "Clinical Research Associate (CRA)" , Eurofins

Get personalized recommendations to optimize your resume specifically for Clinical Research Associate (CRA). Takes only 15 seconds!

AI-powered keyword optimization
Skills matching & gap analysis
Experience alignment suggestions

Check Your ATS Score for "Clinical Research Associate (CRA)" , Eurofins

Find out how well your resume matches this job's requirements. Get comprehensive analysis including ATS compatibility, keyword matching, skill gaps, and personalized recommendations.

ATS compatibility check
Keyword optimization analysis
Skill matching & gap identification
Format & readability score

Answer 10 quick questions to check your fit for Clinical Research Associate (CRA) @ Eurofins.

Quiz Challenge
10 Questions
~2 Minutes
Instant Score

Related Books and Jobs

No related jobs found at the moment.