Clinical Research Associate
vor 4 Wochen
We are a research-driven biopharmaceutical company. Our mission is built on the simple premise that if we “follow the science” that great medicines can make a significant impact to our world. We believe that a research-driven enterprise dedicated to world-class science can succeed by inventing medicine and vaccine innovations that make a difference for patients across the globe.
Our Clinical Research and Pharmacovigilance team push the boundaries of global healthcare through research and innovation. Through clinical trials and surveillance, we ensure the safety and efficacy of our existing and pipeline products to produce safe, effective, innovative medicine.
We are continually striving to improve the understanding of health care within the local community. Our site in 1100 Vienna (ICON Tower) is a strategic location for the distribution of our high quality and innovative health care products, as well as digitally integrated solutions for our patients and clients. To ensure sustainable company growth, we continually aim to offer attractive career opportunities for more than 170 employees at our Vienna site.
Clinical Research Associate (m/f/d)
As a Clinical Research Associate and under the supervision of the CRA Manager, you will ensure compliance of the studies conducted with ICH/GCP and country regulations, company policies and procedures, quality standards as well as adverse event reporting requirements internally and externally. You will act as the primary point of contact for the study sites and the site managers throughout all phases of the clinical research studies, taking overall responsibility of the allocated sites. On this rile you will actively develop and expand the territory for clinical research, finding and developing new sites and you will act as the subject matter expert for monitoring processes and systems.
Aufgaben
Responsibilities
Primary site contact and responsible for site management and monitoring activities throughout all study phases from validation to close-out. Assisting the allocated sites with all open matters and requests (remote and on-site) Collection of regulatory documents and management of data in various clinical trial systems Ensuring study conduct is in compliance with all relevant regulations and standards Ability to serve as a subject matter expert for monitoring processes/systems and supporting the team on a local or global level
Anforderungen
Qualifications
Previous experience working as a Clinical Research Associate (CRA) Enjoys a high level of personal responsibility and readily supports site staff on-site including the required travels High affinity in examining medical data and source documents Detail-oriented and efficient in time management and ability to prioritize Strong communication and presentation skills Flexible and enjoys supporting sites on a path of constant change Excellent verbal and written communication skills in English and German-
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