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Salary
$29k – $76k per year (Estimated)
Location
Remote (Germany)
Seniority
Middle · 2+ years exp
Employment
Full-Time
Overview
Company
Impact
Profile match
Eurofins Scientific is a laboratory testing group founded in 1987 to commercialise a method for authenticating the origin of wines and foods, and it has since become one of the largest bioanalytical testing networks in the world. It runs thousands of laboratories offering food and feed testing, environmental analysis, pharmaceutical and biopharma product testing, agroscience services, clinical diagnostics and consumer product certification. The group is registered in Luxembourg, listed in Paris, and has grown almost entirely by acquiring and integrating specialist laboratories across more than sixty countries.

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.

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

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

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

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