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

IQVIA; United States; Remote; USD 39,000 - 47,000; Full time

Benefits offered by this job

Home office

Company car

Accident insurance

Job summary

IQVIA is seeking a Clinical Research Associate I or II (m/w/d) to work home-based across Austria in our single sponsor department. You will gain direct exposure to client teams and a broad range of therapeutic areas while benefiting from world-class training and mentoring.

You’ll perform site visits, support recruitment planning, ensure GCP/ICH compliance, manage regulatory submissions and data queries, and collaborate with study sites. Travel up to 40-60% may be required.

Qualifications

• University degree in life science or health care field.
• At least one year of on-site monitoring experience.
• Knowledge of GCP/ICH guidelines.
• Fluency in German (C1) and good command of English.
• Driver’s license class B.

Responsibilities

• 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 guidelines.
• Managing regulatory submissions, recruitment, CRF completion, and data query resolution.
• Collaborating with study sites and client representatives.
• Remote monitoring, study start-up involvement, or therapeutic-area specialization as applicable.
• Mentoring less experienced team members and providing subject matter support.

Skills

German fluency

English proficiency

Communication skills

Attention to detail

Education

Life science degree or healthcare apprenticeship

Job description

Join IQVIA as a Clinical Research Associate I or II (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.

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
• Preferable of one year 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 3.400 EUR basic - an overpay according to skills and working experience is possible

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.