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

IQVIA; Remote; EUR 50.000 - 70.000; Vollzeit

Zusammenfassung

A leading global contract research organization is seeking a Clinical Research Associate 2 to work home-based throughout Germany. This role includes responsibilities such as site monitoring, managing regulatory compliance, and mentoring team members. Candidates should have a degree in life sciences, fluency in German at C1 level, and a minimum of 2-4 years of on-site monitoring experience. The position offers a permanent contract with flexible work schedules and resources for career growth.

Leistungen

Permanent contract

Home-Office and flexible work schedules

Company car

Accident insurance

Qualifikationen

• Two to four years of on-site monitoring experience.
• Knowledge of GCP and ICH guidelines.
• Flexibility to travel up to 40-60% of working time.
• Driver’s license class B.

Aufgaben

• 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.
• Managing progress by tracking regulatory submissions.
• Collaborating with experts at study sites and client representatives.
• Mentoring of less experienced team members.

Kenntnisse

Site monitoring

Regulatory compliance

Communication skills

Attention to detail

Fluency in German

Fluency in English

Ausbildung

University Degree in life science or equivalent

Apprenticeship in the health care field

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.

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.com