Clinical Research Associate 1 or 2 (m/w/d), Single Sponsor

IQVIA; Frankfurt; Hybrid; EUR 50,000 - 70,000; Full time

Benefits offered by this job

Company car or car allowance

Accident insurance

Pension

Flexible working schedules

Job summary

IQVIA LLC is seeking a Clinical Research Associate 1 or 2 to work home-based throughout Germany. The role involves site selection, monitoring, and ensuring compliance with regulatory requirements.

Candidates should have at least 12 months of on-site monitoring experience, a relevant university degree, and fluent German (C1). The position offers a permanent contract with competitive salary, home-office options, and resources for career growth.

Qualifications

• Minimum of 12 months of on-site monitoring experience.
• Strong written and verbal communication skills.
• Attention to detail and ability to work in a fast-paced environment.

Responsibilities

• Perform site selection, initiation, monitoring and close-out visits.
• Support the development of a subject recruitment plan.
• Track regulatory submissions, recruitment, and data query resolution.

Skills

Site selection and initiation

Monitoring and close-out visits

Knowledge of GCP and ICH guidelines

Fluency in German (C1)

Communication skills

Education

University Degree in life science or health care

Job description

## Clinical Research Associate 1 or 2 (m/w/d), Single SponsorApplylocations: Frankfurt, Hesse, Germanytime type: Full timeposted on: Posted Todayjob requisition id: R1548524Join 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.* 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.comIQVIA 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.