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

IQVIA LLC; Frankfurt; Remote; EUR 45,000 - 65,000; Full time

Benefits offered by this job

Company car or car allowance

Home-office and flexible schedules

Job summary

IQVIA LLC is hiring a Clinical Research Associate I/II to work remotely across Germany. You will perform site visits, support recruitment planning, and ensure regulatory adherence under GCP/ICH guidelines.

Join a leading global CRO with strong training, mentoring, and career development as you gain experience across therapeutic areas, while enjoying home-based flexibility and continuous learning opportunities.

Qualifications

• Degree or healthcare apprenticeship.
• Strong written and verbal communication skills.
• Fluency in German (C1) and good English proficiency.

Responsibilities

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

Skills

Communication skills

German (C1)

English proficiency

Travel willingness

Education

University degree in life science or healthcare apprenticeship

Job description

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.

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 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.

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.