Qualifications Registered Nurse, other healthcare professional, or Clinical Research Associate (CRA) required.High flexibility to travel (including internationally if needed).Bachelor’s degree (BA/BS) in Health Sciences or related field, or equivalent qualifications.Located in Germany with fluency in German and English languages.1–2 years of relevant direct experience in working with research sites.Clinical competence in the therapeutic area.Excellent interpersonal and communication skills.Strong written and verbal communication skills.Ability to work independently and coordinate across multiple functions.Solutions-oriented approach and positive attitude.Strong customer service orientation and collaborative mindset.Demonstrates empathy and cultural awareness.Upholds the values of IQVIA and the CTE group.
Joining the team provides the opportunity to work with the preparation and documentation of clinical research projects in different therapeutic areas in Germany or the DACH region. You will be involved in data management, creation of study related documents and correspondence with internal departments, research sites and our client to ensure a complete and accurate Trial Master File delivery.
Join IQVIA as a CRA II / SrCRA (m/w/d) in our Clinical Site Management department home-based throughout Germany. You will focus on a comprehensive clinical trial management in a variety of indications and learn about the diverse scientific approach of the sponsors.
We currently offer the exciting opportunity to join the team as Local Trial Manager (m/w/d) in full-time and work home-based throughout Germany. Your responsibilities will include: Services rendered will adhere to applicable company’s standard operating procedures (SOPs), work instructions, policies, codes of Good Clinical Practice (GCP), local regulatory requirements, etc.Prepare or contribute to high level budget estimate in response to Request for Service’s followed by detailed budget proposal.
Join IQVIA as a Clinical Research Associate 1 or Clinical Research Associate 2 / CRA I or CRA II and work home-based throughout Germany in our single sponsor department. You will enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our clients.
Join IQVIA as a Clinical Research Associate 2 / CRA 2 or as Senior Clinical Research Associate 1 / SrCRA 1 (m/w/d) and work home-based throughout Germany in our single sponsor department. You will enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our clients.
Raymond Netzwerks, das mit Fertigungsbetrieben weltweit präsent ist, sind wir mit unseren Produkten aus Metall und Kunststoff ein international führendes und erfolgreiches, innovatives Unternehmen auf dem Weltmarkt für Spezialbefestigungssysteme. ARaymond Fluid Connection Germany GmbH Personalwesen Max-Immelmann-Allee 25 79427 Eschbach Weitere Informationen zum Unternehmen erhalten Sie auf unserer Homepage https://www.araymond.com
Join IQVIA Biotech as a Clinical Research Associate 2 / CRA 2 (m/w/d) to work home-based throughout Germany, and preferably in the Munich or Hamburg area. You will enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with our clients.
What we offer: 3 months lasting internship opportunity based in Germany (next possible start date: May. 2026).Remote work / home office with high-class remote trainings and guidance combined with work experience - remote and on business travel.The aim is a training on the Clinical Research Associate role, there might be an option to offer a permanent employment in this field afterwards.Collecting knowledge: in basic remote and practical on-site trainings in clinical research.Gaining a brought work experience in the administration of clinical trials: supporting the Clinical Trials Assistants with documentation and filing, accompanying the Clinical Research Associates to various visit types at the research sites (onsite and remote visits, including administration), assisting the Study Start-Up Group with relevant documents for Ethical Committees and contracting purposes.Working with the latest computer systems and first-class IT equipment.
What we offer: 3 months lasting internship opportunity based in Germany (next possible start date: May. 2026).Remote work / home office with high-class remote trainings and guidance combined with work experience - remote and on business travel.The aim is a training on the Clinical Research Associate role, there might be an option to offer a permanent employment in this field afterwards.Collecting knowledge: in basic remote and practical on-site trainings in clinical research.Gaining a brought work experience in the administration of clinical trials: supporting the Clinical Trials Assistants with documentation and filing, accompanying the Clinical Research Associates to various visit types at the research sites (onsite and remote visits, including administration), assisting the Study Start-Up Group with relevant documents for Ethical Committees and contracting purposes.Working with the latest computer systems and first-class IT equipment.
Associate Director, Biostatistics - Permanent - w /m / d Global Biostatistics Home-Based/Hybrid: Germany Join us on our exciting journey! The Global Biostatistics (Data Sciences, Safety & Medical) team at IQVIA are experienced in submissions for all major regions; working together with key groups such as, Global Regulatory Affairs, Safety, Project and Data Management, and Medical Writing, to drive efficiency and accountability.
You will work in international development teams from Germany, Denmark, and Malaysia as well as with external partners, users, physicians, and suppliers. Suggested candidate profile Skills and experience can be earned in many different ways, and we understand that the best fit for the role cannot be prescribed on paper.