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Jobs in Wiesbaden, Germany

Senior Clinical Research Associate I (m/w/d), Single Sponsor

IQVIA

Germany
Remote
EUR 60,000 - 80,000
30+ days ago
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Vertriebsexperte Gastronomie (all genders) – SaaS-Vertrieb aus dem Homeoffice

gastronovi GmbH

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EUR 45,000 - 60,000
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Account Executive (SaaS Sales)

Zync.

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EUR 50,000 - 80,000
30+ days ago

Account Manager und Anwendungstechniker (m/w/d) duroplastische Kunststoffe

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Seevetal
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EUR 60,000 - 80,000
30+ days ago

AUGENOPTIKERMEISTER ODER

LasikCare

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EUR 40,000 - 55,000
30+ days ago
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Genossenschaftsverband - Verband der Regionen e.V.

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Genossenschaftsverband - Verband der Regionen e.V.

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EUR 60,000 - 80,000
30+ days ago
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Senior Clinical Research Associate I (m/w/d), Single Sponsor
IQVIA
Germany
Remote
EUR 60.000 - 80.000
Full time
30+ days ago

Job summary

Join a leading global contract research organization as a Senior Clinical Research Associate in Germany. This home-based role offers professional development in clinical research, with responsibilities including site monitoring and collaboration with study sites. Ideal candidates will have a degree in life sciences and substantial on-site monitoring experience, as well as fluency in German.

Benefits

Home-office
Company car
Accident insurance
Flexible work schedules

Qualifications

  • Minimum of four years of on-site monitoring experience.
  • Fluency in German (C1 level) and good command of English.
  • Driver’s license class B.

Responsibilities

  • Perform on-site monitoring, including initiation and close-out visits.
  • Develop subject recruitment plans and evaluate site practices.
  • Mentor less experienced team members.

Skills

Communication
Attention to detail
Life science knowledge
Regulatory standards knowledge

Education

University Degree in life science or scientific discipline
Apprenticeship in the health care field
Job description

Join IQVIA as a Senior Clinical Research Associate I / Sr CRA 1 (m/w/d) home-based throughout Germany in our single sponsor department, and advance your career in clinical research. You’ll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our clients. Whether you're just starting out or looking to deepen your expertise, this role promises to offer intentional career growth and professional development. With access to world-class training and mentoring, you’ll have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas.

Your responsibilities will include:

  • Performing site selection, initiation, monitoring and close-out visits
  • Supporting the development of a subject recruitment plan
  • Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
  • Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
  • Collaborating with experts at study sites and with client representatives
  • Depending on client model there might be remote-monitoring, involvement in study start-up processes, specialization on therapeutic area (pharmaceutical product or medical devices)
  • Mentoring of less experienced team members, support as subject matter expert for specific topics or additional tasks might be included

Qualifications:

  • University Degree in life science or other scientific discipline or apprenticeship in the health care field
  • Minimum of four years of on-site monitoring experience alternatively an equivalent combination of education, training and experience
  • Knowledge of applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
  • Strong written and verbal communication skills, attention to detail and ability to work in a fast pace environment
  • Fluency in German on at least C1 level and a good command of English
  • Flexibility to travel up to 40-60% of working time
  • Driver’s license class B

What you can expect:

  • Resources that promote your career growth
  • Leaders that support flexible work schedules
  • Programs to help you build your therapeutic knowledge
  • Dynamic work environments that expose you to new experiences
  • Home-office, company car, accident insurance and more

Whatever your career goals, we are here to ensure you get there!

Please apply with your English CV and motivation letter.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

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* The salary benchmark is based on the target salaries of market leaders in their relevant sectors. It is intended to serve as a guide to help Premium Members assess open positions and to help in salary negotiations. The salary benchmark is not provided directly by the company, which could be significantly higher or lower.

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