채용
Benefits & Perks
•Remote Work
•Flexible Hours
•Home Office Stipend
•Commuter Benefits
•Learning Budget
•Remote Work
•Flexible Hours
•Home Office
•Commuter
•Learning
Required Skills
Clinical Research Associate
Site Monitoring
GCP
ICH Guidelines
German Language
English Language
Join IQVIA as a Clinical Research Associate I or II (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 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 oneyear of on-site monitoring 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
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Fluency in German on at least C1 level and a good command of English
-
Flexibility to travel up to 40-60% of working time
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Driver’s license class BWhat 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
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Monthly gross salary: starting at 3.600 EUR basic - an overpay according to skills and working experience is possible
Whatever your career goals, we are here to ensure you get there!
We invite you to join IQVIA™.Please apply with your English CV, motivation letter and your certificates and reference letters.
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.
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About IQVIA

IQVIA
PublicFocused on health information technology and clinical research.
10,001+
Employees
Durham
Headquarters
$17B
Valuation
Reviews
3.9
2 reviews
Work Life Balance
2.5
Compensation
2.0
Culture
2.8
Career
3.0
Management
2.5
65%
Recommend to a Friend
Pros
Structured feedback and development process
Meaningful contribution to client businesses
Problem-solving with specialized knowledge
Cons
Strict performance requirements and termination risk
High-level rubric definitions lack detail
No performance bonuses offered
Salary Ranges
42 data points
Junior/L3
Senior/L5
Junior/L3 · Analyst
2 reports
$107,910
total / year
Base
$93,834
Stock
-
Bonus
-
$97,750
$118,068
Interview Experience
3 interviews
Difficulty
3.0
/ 5
Duration
14-28 weeks
Experience
Positive 0%
Neutral 33%
Negative 67%
Interview Process
1
Application Review
2
HR Screen
3
Hiring Manager Interview
4
Technical Manager Interview
5
Executive/GM Interview
6
Offer
Common Questions
Behavioral/STAR
Case Study
Technical Knowledge
Past Experience
Culture Fit
News & Buzz
IQVIA Holdings Collaboration With Boehringer Ingelheim Supports Undervalued Thesis - simplywall.st
Source: simplywall.st
News
·
5w ago
Ritter Daniher Financial Advisory LLC DE Acquires Shares of 4,267 IQVIA Holdings Inc. $IQV - MarketBeat
Source: MarketBeat
News
·
5w ago
IQVIA and Boehringer Ingelheim collaborate on therapeutic data transformation - Pharmaceutical Business review -
Source: Pharmaceutical Business review -
News
·
5w ago
IQVIA to Share its DaaS+ Platform in Boehringer Ingelheim Collaboration - Contract Pharma
Source: Contract Pharma
News
·
5w ago