Senior Clinical Research Associate II/III (m/w/d), Multi-Sponsor, Germany

IQVIA; Frankfurt; Teletrabalho; EUR 55 000 - 75 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Home-office

Company car / car allowance

Accident insurance

Pension

Resumo da oferta

IQVIA invites a Senior CRA II/III to join its Clinical Site Management team, working home-based across Germany. The role focuses on comprehensive trial management, regulatory compliance, and strong cross‑functional collaboration with study teams and investigators.

You will monitor complex trials, support site relationships, and contribute to recruitment planning while traveling up to 60% and maintaining high standards of GCP and ICH adherence. IQVIA provides a diverse, global environment.

Qualificações

• On-site monitoring experience is required.
• Knowledge of GCP and ICH guidelines.
• Ability to travel up to 60% of working time.
• Fluency in German and English.

Responsabilidades

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

Conhecimentos

German language

English language

Strong communication

Attention to detail

Travel flexibility

Formação académica

University degree in life sciences or health care apprenticeship

Descrição da oferta de emprego

Join IQVIA as a SrCRA II/III (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. With strategic site relationship managers supporting you throughout your role, this is a fantastic opportunity for you to embed yourself in the wider clinical operations team and work on ground-breaking new medicine development.

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 Harmonisation (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 six years of on-site monitoring experience.
• Knowledge of applicable clinical research regulatory requirements i.e., GCP and ICH guidelines.
• Strong written and verbal communication skills, attention to detail and ability to work in a fast pace environment.
• Good 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.

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.