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IQVIA
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Clinical Research Associate 2 (m/w/d), IQVIA Biotech, based in Austria
Austria
· Full-time
·
Not Applicable
External Job Description
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. This role promises to offer intentional career growth and professional development. 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 and in covering projects in Austria, Germany and/or Switzerland.
Your Responsibilities Will Include
Whatever your career goals, we are here to ensure you get there!
Please apply with your English CV and motivation letter as well as your education certificates and job reference letters (Arbeitszeugnisse).
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
IQVIA 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.
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. This role promises to offer intentional career growth and professional development. 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 and in covering projects in Austria, Germany and/or Switzerland.
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.
- Mentoring of less experienced team members, support as subject matter expert for specific topics or additional tasks might be included.
- University Degree in life science or other scientific discipline or apprenticeship in the health care field.
- Minimum of two 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 conduct business travel in Austria, Germany and/or Switzerland up to about 40-60% of working time.
- Driver’s license class B.
- Permanent contract.
- Home-Office and flexible work schedules.
- Resources that promote your career growth.
- Company car, accident insurance and more.
- Monthly gross salary: starting at 4.000 EUR basic - an overpay according to skills and working experience is possible.
Whatever your career goals, we are here to ensure you get there!
Please apply with your English CV and motivation letter as well as your education certificates and job reference letters (Arbeitszeugnisse).
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
IQVIA 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.
Key Skills
Ranked by relevance
gcp
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- Posted
- Mar 18, 2026
- Type
- Full-time
- Level
- Not Applicable
- Location
- Vienna
- Company
- IQVIA
Industries
Hospitals
Health Care
Categories
Research
Analyst
Information Technology
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