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

IQVIA; United States; Remote; USD 40,000 - 48,000; Full time

Benefits offered by this job

Home-office

Company car

Accident insurance

Pension

Job summary

IQVIA is seeking a CRA or SrCRA to join our Clinical Site Management team, operating from home across Austria. You will monitor complex trials and ensure adherence to GCP/ICH while building strong relationships with the global study team and investigators.

Your responsibilities include site selection, initiation, monitoring, recruitment planning, regulatory tracking, and collaboration with client representatives. Up to 70% travel may be required.

Qualifications

• Life science degree or health care apprenticeship.
• Experience as CRA, Study Coordinator/Nurse or Clinical Trial Coordinator is required.
• Knowledge of GCP/ICH guidelines.

Responsibilities

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

Skills

German & English

Strong communication

Education

Life science degree

Health care apprenticeship

Job description

Join 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!

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.