(Senior) Clinical Research Associate (s)CRA - sponsor-dedicated

Job Overview:

(Senior) Clinical Research Associate (s)CRA - sponsor-dedicated

Location: Vienna, Austria / Home Office, Austria

A formula for clinical innovation: Covance + LabCorp. With comprehensive drug development services and de-identified data from 70 million patients worldwide, our 60,000 employees advance life-changing medicines across a wide range of therapeutic areas. In this role, you will work directly with one of our renowned key sponsors and advance the development of innovative, life-changing medications for oncological therapies.

What we have to offer: a strong international support network, flexible working solutions that facilitate a genuine work-life balance, excellent career opportunities, a highly competitive compensation package and the opportunity to significantly raise your profile in the industry.

If you are looking to broaden your therapeutic expertise whilst gaining exposure within a world-class pharmaceutical working environment, we are looking forward to meeting you!

As (Senior) Clinical Research Associate, you typically will: Own all aspects of site management as described in the project plans Ensure the study staff conducting the protocol receive all materials and instructions to safely enter patients into the study Protect study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document review. Monitor data for missing or implausible entries Perform the required monitoring tasks in an efficient manner, according to SOPs and established guidelines; prepare accurate and timely trip reports Review progress of projects and initiate appropriate actions to achieve target objectives Interact with internal work groups to evaluate needs, resources and timelines Act as contact for clinical trial suppliers and other vendors as assigned Complete process of Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs Independently perform CRF reviews Generate queries and resolve issues according to data review guidelines on Covance or sponsor data management systems Assist with training, mentoring and development of new employees, e.g. co-monitoring Education/Qualifications:Degree in a relevant field such as life sciences, pharmacology, (veterinarian) medicine, oecotrophology etc. or an equivalent scientific or commercial Higher Vocational education (e.g. study nurse, study coordinator) Experience:Solid experience in clinical research in a variety of therapeutic areas including Oncology Previous monitoring experience in Austria and familiarity with applicable Austrian regulations and authorities Awareness of applicable clinical research regulatory requirements such as Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) Working knowledge of Microsoft Word, Excel and PowerPoint Effective time management and organizational skills and a keen attention to detail Ability to establish and maintain effective, trustful working relationships with internal and external stakeholders Business fluency in German - both spoken and written - as well as a good command of English are a must