MNC InsiderMNC Insider

Junior CRA (m/w/d), Single Sponsor, home-based Austria

IQVIA

Junior CRA (m/w/d), Single Sponsor, home-based Austria

full-timePosted: Sep 1, 2026Austria, Vienna

Job Description

Join IQVIA as a Junior CRA (m/w/d) home-based throughout Austria 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 visitsSupporting the development of a subject recruitment planEvaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelinesManaging progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolutionCollaborating with experts at study sites and with client representativesDepending 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 includedQualifications: University Degree in life science or other scientific discipline or apprenticeship in the health care fieldKnowledge of applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelinesStrong written and verbal communication skills, attention to detail and ability to work in a fast pace environmentFluency in German on at least C1 level and a good command of EnglishFlexibility to travel up to 40-60% of working timeDriver’s license class BWhat you can expect: Resources that promote your career growthLeaders that support flexible work schedulesPrograms to help you build your therapeutic knowledgeDynamic work environments that expose you to new experiencesHome-office, company car, accident insurance and moreMonthly gross salary: starting at 3.200 EUR basic - an overpay according to skills and working experience is possibleWhatever 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.comIQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Locations

  • Austria, Vienna

Skills Required

  • applicable clinical research regulatory requirements iintermediate
  • German on at least C1 levelintermediate

Required Qualifications

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

Responsibilities

  • 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
  • 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

Target Your Resume for "Junior CRA (m/w/d), Single Sponsor, home-based Austria" , IQVIA

Get personalized recommendations to optimize your resume specifically for Junior CRA (m/w/d), Single Sponsor, home-based Austria. Takes only 15 seconds!

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

Check Your ATS Score for "Junior CRA (m/w/d), Single Sponsor, home-based Austria" , IQVIA

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

Tags & Categories

GeneralGeneral

Answer 10 quick questions to check your fit for Junior CRA (m/w/d), Single Sponsor, home-based Austria @ IQVIA.

Quiz Challenge
10 Questions
~2 Minutes
Instant Score

Related Books and Jobs

No related jobs found at the moment.