Clinical Research Associate 2 (mwd), IQVIA Biotech

IQVIA; Remote; EUR 45.000 - 60.000; Vollzeit

Zusammenfassung

A leading global contract research organization is seeking a Clinical Research Associate 2 to work home-based throughout Germany. The role involves site monitoring, supporting recruitment plans, and ensuring compliance with regulatory requirements. Candidates should have a degree in life sciences, at least two years of on-site monitoring experience, and fluency in German (C1). The position offers a permanent contract, flexible work schedules, and resources for career growth.

Leistungen

Permanent contract

Home-Office and flexible work schedules

Company car accident insurance

Resources that promote career growth

Qualifikationen

• Minimum of two years of on-site monitoring experience or equivalent.
• Knowledge of GCP and ICH guidelines.
• Flexibility for business travel up to 40-60%.

Aufgaben

• Perform site selection, initiation, monitoring, and close-out visits.
• Support the development of a subject recruitment plan.
• Evaluate quality and integrity of site practices according to regulatory requirements.
• Manage tracking of regulatory submissions and data query resolution.
• Mentor less experienced team members.

Kenntnisse

Fluency in German at C1 level

Strong written and verbal communication skills

Attention to detail

Ability to work in a fast-paced environment

Ausbildung

University degree in life science or equivalent

Jobbeschreibung

Clinical Research Associate 2 / CRA 2

Join IQVIA Biotech as a Clinical Research Associate 2 / CRA 2 (m/w/d) to work home-based throughout Germany and preferably in the Munich or Hamburg area.

You will enjoy the stability and resources of a leading global contract research organization while gaining direct experience with our clients. This role promises to offer intentional career growth and professional development. Youll 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 and in covering projects in Germany Austria and Switzerland.

Responsibilities

• Perform site selection, initiation, monitoring, and close-out visits.
• Support the development of a subject recruitment plan.
• Evaluate the quality and integrity of site practices in accordance with regulatory requirements (GCP, ICH).
• Manage progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution.
• Collaborate with experts at study sites and with client representatives.
• Mentor 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 years of on-site monitoring experience or an equivalent combination of education, training, and experience.
• Knowledge of applicable clinical research regulatory requirements (GCP, ICH guidelines).
• Strong written and verbal communication skills, attention to detail, and ability to work in a fast-paced environment.Fluency in German at C1 level and a good command of English.
• Flexibility to conduct business travel up to about 40-60% of working time.
• Driver’s license class B.

Benefits

• Permanent contract.
• Home-Office and flexible work schedules.
• Company car accident insurance and more.
• Resources that promote your career growth.

We invite you to join IQVIA.

Whatever your career goals we are here to ensure you get there!

Application

Please apply with your English CV and motivation letter as well as your education certificates and job reference letters (Arbeitszeugnisse).