CRA II or SrCRA I (m/w/d), Single Sponsor, home-based Austria

IQVIA LLC; Wien; Remote; EUR 43.000 - 51.000; Vollzeit

Benefits dieser Stelle

Home-office

Company car

Accident insurance

Flexible work schedules

Zusammenfassung

IQVIA LLC is hiring Clinical Research Associate II or Senior CRA I (m/w/d) for a home-based role across Austria. You will monitor sites, support recruitment, ensure GCP/ICH compliance, and collaborate with client teams within a single sponsor department.

Up to 60% travel may be required, with strong training and career growth opportunities. The role offers exposure to multiple therapeutic areas, mentoring, and a pathway to seniority in a global CRO environment.

Qualifikationen

• University degree in life sciences or related field or healthcare apprenticeship.
• At least two years of on-site monitoring experience.
• Knowledge of GCP/ICH regulatory requirements.
• Strong written and verbal communication, attention to detail, and ability to work in a fast-paced environment.
• German at C1 level and good English.
• Willingness to travel 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 site practices for compliance with GCP/ICH.
• Tracking regulatory submissions, recruitment, CRF completion, and data query resolution.
• Collaborating with study sites and client representatives.
• Possible remote-monitoring, study start-up involvement, or therapeutic area specialization.
• Mentoring less experienced team members and providing SME input.

Kenntnisse

GCP/ICH knowledge

German (C1) & English

Strong communication

Attention to detail

Travel willingness 40-60%

Driver's license B

Ausbildung

University degree in life sciences or healthcare apprenticeship

Jobbeschreibung

Join IQVIA as a Clinical Research Associate II or Senior Clinical Research Associate I (m/w/d) home-based throughout Austria 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.

Responsibilities

• 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 years of on‑site monitoring 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

• 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 and more
• Monthly gross salary: starting at 4.200 EUR basic - an overpay according to skills and working experience is possible

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.

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.