Clinical Research Associate 1 or 2 (m/w/d), Multi-Sponsor, Germany

IQVIA, Inc.; Frankfurt; Sur place; EUR 65 000 - 82 000; Plein temps

Avantages offerts par ce poste

Home-office

Company car/car allowance

Accident insurance

Pension

Résumé du poste

IQVIA is seeking a CRA 1 or CRA 2 (m/w/d) for home-based work across Germany. You will monitor complex clinical trials, ensure adherence to GCP and study protocols, and collaborate with the global study team and investigators.

Responsibilities include site visits (selection, initiation, monitoring, close-out), developing recruitment plans, and regulatory tracking. Required: life science degree or healthcare apprenticeship, 1 year on-site monitoring or equivalent, fluent German and English, and

Qualifications

• Fluent command of German and English (written and spoken).
• Life science degree or apprenticeship in healthcare.
• Minimum of one year on-site monitoring experience, or equivalent as Study Coordinator/CTC.

Responsabilités

• Perform site selection initiation monitoring and close-out visits.
• Support development of a subject recruitment plan.
• Evaluate site practices for GCP/ICH compliance and data integrity.
• Track regulatory submissions, recruitment, CRF completion and data queries.
• Collaborate with site teams and client representatives.

Connaissances

German and English

Attention to detail

Strong communication

Formation

Life science degree

Healthcare apprenticeship

Description du poste

Join IQVIA as a CRA 1 or CRA 2 (m/w/d) in our Clinical Site Management department home-based throughout Germany. You will focus on a comprehensive clinical trial management in a variety of indications and learn about the diverse scientific approach of the sponsors. Beside establishing strong relationships with the global study team and the involved investigators, you will conduct monitoring on complex clinical trials for different pharma companies and assure their adherence to good clinical practices and study protocols.

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 on study sites and client representatives.

Qualifications:

• University Degree in life science or other scientific discipline or apprenticeship in health care.
• Minimum of one year of on-site monitoring experience, alternatively miminum one year experience as Study Coordinator/CTC etc.
• 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.
• Fluent command of German and English.
• Flexibility to business travel up to 60% of working time.
• Driver's license class B.

What you can expect:

• Resources that promote your career growth.
• Leaders that support flexible work schedules.
• Programs to help you build your therapeutic knowledge.
• Dynamic work environments that expose you to new experiences.
• Home-office, company car/car allowance, accident insurance, pension and more.

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

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.