Clinical Research Associate 1 or 2 (m/w/d), Multi-Sponsor, Germany

IQVIA; Frankfurt; Hybrid; EUR 48,000 - 72,000; Full time

Benefits offered by this job

Home office

Company car or car allowance

Accident insurance

Pension plan

Job summary

IQVIA LLC is seeking a CRA 1/CRA 2 (m/w/d) to operate home-based across Germany. You will manage clinical trial activities, ensure GCP/ICH adherence, and build strong relationships with global study teams and investigators.

You will conduct monitoring visits, support recruitment planning, and track regulatory submissions while collaborating with site staff and sponsors in a fast-paced environment. Sprachkenntnisse in German und Englisch required.

Qualifications

• University Degree in life science or other scientific discipline or apprenticeship in health care.
• Minimum of one year of on-site monitoring experience, alternatively minimum one year experience as Study Coordinator/CTC.
• Knowledge of 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.
• Fluent command of German and English.
• Flexibility to business travel up to 60% of working time.
• Driver’s license class B.

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 on study sites and client representatives.

Skills

On-site monitoring

GCP/ICH knowledge

Regulatory compliance

German fluency

English fluency

Travel up to 60%

Driver’s license

Education

Life science degree

Healthcare apprenticeship

Job description

Join IQVIA as a CRA 1 or CRA 2 (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. Beside establishing strong relationships with the global study team and the involved investigators, you will conduct monitoring on complex clinical trials for different pharma companies and assure their adherence to good clinical practices and study protocols. With strategic site relationship managers supporting you throughout your role, this is a fantastic opportunity for you to embed yourself in the wider clinical operations team and work on ground-breaking new medicine development.

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 on study sites and client representatives.

Qualifications:

• University Degree in life science or other scientific discipline or apprenticeship in health care.
• Minimum of one year of on-site monitoring experience, alternatively miminum one year experience as Study Coordinator/CTC etc.
• 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.
• Fluent command of German and English.
• Flexibility to business travel up to 60% of working time.
• Driver’s license class B.

What 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/car allowance, accident insurance, pension and more.

Whatever your career goals, we are here to ensure you get there!

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.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.

To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact.

No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere.

Thank you for your interest in growing your career with us.