AT-Clinical Trial Associate

QPS Holdings, LLC; Graz; Vor Ort; EUR 40 000 - 55 000; Vollzeit

Zusammenfassung

A prominent contract research organization in Graz, Austria, is seeking a Clinical Trial Associate for a temporary position. The role involves maintaining clinical trial documentation and supporting project managers in various administrative tasks. Applicants should have a medical or natural scientific background and fluency in both English and German. This position demands attention to detail and the ability to work to deadlines, making it a perfect opportunity for a qualified candidate eager to contribute to clinical research.

Qualifikationen

• Business level fluency in English and German required.
• Must have a medical or natural scientific background.
• Local candidate able to work onsite regularly.

Aufgaben

• Maintain and coordinate logistics of clinical trials according to regulations.
• Set up and organize clinical study documentation.
• Attend project team meetings and assist with coordination tasks.

Kenntnisse

Fluency in English

Fluency in German

Team Player

Project Management

Attention to Detail

Ausbildung

Medical or Natural Science Background

Jobbeschreibung

Clinical Trial Associate in Graz, Austria

Temporary Graz, Steiermark, AT

3 days ago Requisition ID: 2882

QPS Austria GmbH is an internationally successful contract research organization in the preclinical and clinical area. The Clinical Research Division handles clinical studies of phases I to IV in all indications. At our location at Brueckenkopfgasse 1, 8020 Graz we are looking for a temporary (~18 months) andoffice based

Clinical Trial Associate (f/m/d)

Your area of responsibility:

The Clinical Trial Associate (CTA) maintains and co-ordinates administrative, financial and logistical aspects of clinical trials according to Good Clinical Practice, relevant SOPs as well as client contracts. The CTA is responsible for project-supporting clinical trial and development tasks.

This function essentially contributes to the accurate documentation and filing of a clinical trial and

acts as a pivotal point of contact for the entire clinical trial team.

The following list provides information on the CTA’s main activities/requirements:

• To provide general administrative support to the Clinical Operations Department and assistance to Project Managers and Clinical Research Associates - covering financial & operative aspects
• To set up, organize and maintain clinical study documentation (e.g. electronic Trial Master File, paper Investigator Site File) including preparation for internal/external audits, final reconciliation and archival
• To attend project team meetings and generate meeting minutes
• To assist the Project Manager and project team with Investigator Meeting coordination, activities preparation and generate meeting minutes
• To assist in the production of slides, overheads, etc., as needed for project presentations.
• To assist with the coordination of team member tracking
• Maintenance of electronic project management systems
• Assist in the preparation, handling and tracking of Ethics/ Regulatory Submissions in the EU (Clinical Trial Information System)
• Coordination of ordering, dispatch and tracking of study material
• To become familiar with regulations for Clinical Trials and Standard Operating Procedures (SOPs)
• Other duties as assigned

Your preferred profile:

• Medical or natural scientific background, if possible
• Must have business level fluency in both English and German (oral/written)
• Good Team Player
• Ability to work to project-driven deadlines
• Accurate and precise working style
• Local candidate, able to work onsite in our Graz, AT offices on a regular basis

For legal reasons, we are obliged to refer to the minimum salary of the collective agreement of the general industry in the management group III. We take your professional and personal skills and relevant professional experience into account when determining the actual salary. We will be happy to discuss the details in person.

If you are interested in this challenging position, please send your application and CV to [e-mail]