CRA 2 (m/w/d), IQVIA Biotech

IQVIA RDS GmbH; Remote; EUR 55.000 - 75.000; Vollzeit

Zusammenfassung

A leading global clinical research organization is seeking a Clinical Research Associate 2 to work home-based throughout Germany. The candidate will be responsible for site selection, monitoring activities, and ensuring compliance with regulatory requirements. Qualifications include a degree in life sciences, 2-4 years of on-site monitoring experience, and fluency in German. The role offers a permanent contract, flexibility in work hours, and opportunities for career growth.

Leistungen

Permanent contract

Home-Office and flexible work schedules

Company car

Accident insurance

Qualifikationen

• Minimum of two-four years of on-site monitoring experience or equivalent.
• Knowledge of GCP and ICH guidelines.
• Driver’s license class B.

Aufgaben

• Perform site selection, initiation, monitoring, and close-out visits.
• Support subject recruitment plan development.
• Evaluate quality and integrity of site practices.
• Manage regulatory submissions and recruitment tracking.
• Collaborate with study site experts and client representatives.
• Mentor less experienced team members.

Kenntnisse

Strong written and verbal communication skills

Attention to detail

Fluency in German (C1)

Good command of English

Flexibility to travel 40–60%

Ausbildung

University Degree in life science or equivalent in health care

2-4 years of on-site monitoring experience

Jobbeschreibung

Join IQVIA Biotech as a Clinical Research Associate 2 / CRA 2 (m/w/d) and work home-based throughout Germany.

You will enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with 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 two‑four years of on‑site monitoring experience alternatively an equivalent combination of education, training and 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 work schedules.




• Company car, accident insurance and more.




• Resources that promote your career growth.

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.com