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Clinical Research Associate 2 (m/w/d), Germany and Switzerland, Single Sponsor
Frankfurt, Hesse, Germany
·
On-site
·
Full-time
·
2w ago
Benefits & Perks
•Flexible Hours
•Remote Work
•Learning Budget
•401(k)
•Healthcare
•Flexible Hours
•Remote Work
•Learning
•401k
•Healthcare
Required Skills
Clinical research
GCP knowledge
ICH guidelines
German language
English language
French language
Join IQVIA as a Clinical Research Associate 2/ CRA II and work home-based in Southern Germany or in the **Frankfurt area **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. Furthermore you will gain experience covering clinical trials in Germany and Switzerland.
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 variety of therapeutic areas.
Your responsibilities will include:
- Performing site selection, initiation, monitoring and close-out visits in Germany and in Switzerland.
- 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 18month 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.
- Fluency in German on at least C1 level and a **good command of English **and French.
- Flexibility to travel up to 40-60% of working time.
- Preferrable
driver’s license class B.What you can expect:
- Permanent contract.
- Home-office and flexible working schedules.
- Competitive salary.
- Company car or car allowance, accident insurance, pension and more.
- Resources that promote your career growth.
- Dynamic work environments that expose you to new experiences.
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.
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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
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