Intern - Legal

AVATR Global Design Center; München; Vor Ort; EUR 42.000 - 66.000; Vollzeit

Benefits dieser Stelle

Permanent contract

Home office & flexible working

Company car or car allowance

Career development & mentoring

Dynamic work environment

Zusammenfassung

IQVIA is hiring a Clinical Research Associate I/II (CRA I/II) to work from home across Germany in a single sponsor department. You will monitor sites, support recruitment planning, and ensure regulatory compliance under GCP/ICH guidelines, with travel up to 40–60% and a driver’s license required.

The role offers professional development and mentoring, with access to training and growth opportunities in a dynamic, global CRO environment.

Qualifikationen

• University degree in life science or health care field.
• Minimum 12 months of on-site monitoring experience.
• Knowledge of GCP and ICH guidelines.
• Fluency in German (C1) and good command of English.
• Willingness to travel 40–60% of time.
• Driver’s license class B.

Aufgaben

• Perform site selection, initiation, monitoring and close-out visits.
• Support development of a subject recruitment plan.
• Evaluate site practices for regulatory compliance (GCP/ICH).
• Manage progress by tracking submissions, recruitment, CRF completion and data queries.
• Collaborate with study sites and client representatives.

Kenntnisse

German (C1) language

English proficiency

Strong communication

Attention to detail

Fast-paced environment

Driver’s license B

Ausbildung

Life science degree or healthcare apprenticeship

Jobbeschreibung

Join IQVIA as a Clinical Research Associate 1 or Clinical Research Associate 2 / CRA I or CRA II and work home-based throughout Germany 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.

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 12 month 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.
• Flexibility to travel up to 40-60% of working time.
• Driver’s license class B.

What you can expect:

• Permanent contract.
• Home-office and flexible working schedules.
• 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!

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.