Clinical Research Associate or SrCRA(m/w/x)

# Clinical Research Associate or SrCRA (m/f/d), Single Sponsor, home-based Switzerland **Basel, Switzerland** | **Full time** Join IQVIA as a **Clinical Research Associate /** **Sr CRA (m/f/d) home-based throughout Switzerland** in our **single sponsor department**, and advance your career in clinical research. You’ll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of 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 **one year 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 * Fluent verbal and written language skills in **German (on at least C1 level)** plus fluent language skills in **French** 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:** * 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, bonus, accident insurance and more Whatever your career goals, we are here to ensure you get there!