Experienced CRA (m/w/d), Multi Sponsor, home-based Austria

IQVIA Inc; Wien; Hybrid; EUR 36,000 - 43,000; Full time

Benefits offered by this job

Home-based position

Company car

Pension plan

Accident insurance

Flexible schedules

Job summary

IQVIA Inc in Vienna, Austria, is hiring a CRA or SrCRA for home-based clinical site management across Austria. You will monitor complex trials for multiple sponsors and ensure adherence to GCP/ICH with a global study team.

Required: life science degree or health care apprenticeship; CRA/coordination experience; German and English proficiency; willingness to travel up to 70%. A valid B-class driving license is needed. We offer flexible schedules and a comprehensive benefits package.

Qualifications

• University degree in life sciences or apprenticeship in health care.
• Experience as CRA, Study Coordinator/Nurse or Clinical Trial Coordinator.
• Knowledge of GCP/ICH guidelines.
• Proficiency in German and English.
• Willingness to travel up to 70%.
• Driver’s license class B.

Responsibilities

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

Skills

CRA Experience

German & English

GCP/ICH knowledge

Travel readiness

Driver's license B

Education

Life science degree or health care apprenticeship

Job description

Experienced CRA (m/w/d), Multi Sponsor, home-based Austria### Experienced CRA (m/w/d), Multi Sponsor, home-based AustriaApply: Vienna, Austria: Full time: Posted Today: R1555200Join IQVIA as a **CRA or SrCRA (m/w/d) in our Clinical Site Management department** home-based throughout Austria. 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 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**.* **Experience as CRA, Study Coordinator/Nurse or Clinical Trial Coordinator is required*** 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.* Good command of **German and English**.* Flexibility to business travel up to 70% 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, accident insurance, pension and more.* Monthly gross salary: starting at 3.500 EUR basic - an overpay according to skills and working experience is possible Whatever your career goals, we are here to ensure you get there! **Please apply with your English CV and motivation letter.**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.comIQVIA 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.