In this clinical research role, you manage remote monitoring and regulatory compliance tasks, support recruitment efforts, and collaborate with study site experts, while also mentoring junior team members.
Anforderungen
- •University Degree in life science
- •Minimum of two years of CRA experience
- •Knowledge of GCP and ICH guidelines
- •Strong written and verbal communication skills
- •Attention to detail
- •Ability to work in a fast pace environment
- •Fluency in German at C1 level
- •Good command of English
- •Driver’s license class B
Deine Aufgaben
- •Perform remote monitoring tasks
- •Support development of subject recruitment plans
- •Evaluate site practices for regulatory compliance
- •Track regulatory submissions and recruitment progress
- •Manage case report form completion and data queries
- •Collaborate with study site experts and client representatives
- •Participate in study start-up processes as needed
- •Mentor less experienced team members
Deine Vorteile
Resources for career growth
Supportive leaders for flexibility
Programs for therapeutic knowledge
Dynamic work environments
Home-office and company car
Original Beschreibung
# Remote Clinical Research Associate (m/w/d), Single Sponsor, home-based Austria
**Vienna, Austria** | **Full time**
Join IQVIA as a **Remote CRA (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:**
* Remote monitoring tasks
* 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 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 CRA 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**
* **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 4.300 EUR basic - an overpay according to skills and working experience is possible