Internship in Clinical Research (m/w/d), Home-Based in Germany

IQVIA; Frankfurt; Remote; EUR 11,000 - 17,000; Part time

Job summary

IQVIA Internship offers a hands-on, project-based experience in a leading global clinical research unit. You will work with the Clinical Trials Team, gaining knowledge in trial administration and documentation while supporting visits and ethical submissions.

The 3-month program in Germany starts February 2027, with remote work options and guidance, plus on-site training. There is potential for permanent employment in the Clinical Research Associate field.

Qualifications

• University degree in life sciences with an advanced training in clinical research is preferred.
• Excellent communication skills in German (C1) and English.
• Strong written and verbal communication skills.
• Proficient in Microsoft Office, especially Excel, and standard internet/communication tools.

Responsibilities

• Support the Clinical Trials Team with documentation and filing for trials.
• Assist Clinical Research Associates during site visits (onsite and remote).
• Support the Start-Up Group with documents for ethics committees and contracting purposes.
• Use latest IT systems and equipment to manage trial-related information.

Skills

German language (C1)

English language

Communication skills

Time management

Education

Life sciences degree

Clinical research training

Tools

Excel

Microsoft Office

Internet tools

Job description

The IQVIA™ Internship provides you with the opportunity to gain relevant, project-based work experience at one of the most successful and cutting-edge global clinical research units in the market while building relationships within the company that will impact your future.

You will be working in our Clinical Trials Team together with some of the most talented people in the field and gain a brought knowledge in the execution of clinical trials.

What we offer:

• 3 months lasting internship opportunity based in Germany (next possible start date: February 2027).
• Remote work / home office with high-class remote trainings and guidance combined with work experience - remote and on business travel.
• The aim is a training on the Clinical Research Associate role, there might be an option to offer a permanent employment in this field afterwards.
• Collecting knowledge: in basic remote and practical on-site trainings in clinical research.
• Gaining a brought work experience in the administration of clinical trials: supporting the Clinical Trials Assistants with documentation and filing, accompanying the Clinical Research Associates to various visit types at the research sites (onsite and remote visits, including administration), assisting the Study Start-Up Group with relevant documents for Ethical Committees and contracting purposes.
• Working with the latest computer systems and first-class IT equipment.

You should have:

• University degree from life science-based subjects preferable plus an advanced theoretical trainings program in clinical research.
• Excellent communication skills in German language (at least C1 level) including good command of English language.
• Strong written and verbal communication skills.
• Computer skills including a high proficiency in use of Microsoft Office applications, especially Excel, internet, and communication tools.
• Excellent organizational and problem-solving skills.
• Effective time management skills and the ability to manage priorities.
• Ability to establish and maintain effective working relationships with coworkers, managers and clients.
• Flexibility to frequent business travel and driving license category B.
• Candidates need to be located in Germany

If you want to make a difference in global healthcare, IQVIA™ is the place for you!

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.