Project Assistance

vor 2 Monaten

Biberach, Deutschland GULP – experts united Vollzeit

Are you a project assistant looking for a new challenge in the pharmaceutical industry ? Are you passionate and committed to your job and always give 100%? So do we The satisfaction of our clients and candidates is our top priority when placing qualified specialists. Randstad professional solutions is currently looking for an employee in the administration of test persons at the Biberach site. Take advantage of this opportunity and apply directly online. We guarantee individual advice, personal support and efficient processing of your application. We welcome people with disabilities.

Here's what we offer

Attractive salary and long-term job security through group affiliation Extensive social benefits, including Christmas and vacation bonuses Vacation entitlement of up to 30 days per year Further training through e.Learning offers Discounts at sports, leisure and wellness facilities

Your tasks

Ensuring the recruitment of test subjects for the clinical studies conducted Maintaining and managing subject files and archive documents Maintenance of the central registration register for study participants Maintenance of the homepage on the Internet Collaboration in the study planning team, incl. assessment of recruitment possibilities and probabilities as part of study planning Preparation of subject and center documents, e.g. supporting the preparation of subject and center documentation for submission to the ethics committee Statistical processing of relevant aspects of clinical trials (e.g. subject statistics, recruitment statistics, incl. source of referral etc.)

Your profile

Completed vocational training in the commercial and/or scientific field (e.g. as a project assistant or study operation staff), preferably with several years of relevant professional experience in the field of clinical trials Confident handling of PCs and electronic applications, in particular MS Office (Outlook, Word and Excel) Secure knowledge of local regulations, GCP and good documentation practice, the corresponding SOPs and the relevant guidelines Fluent German and good written and spoken English skills Friendliness and enjoyment of contact with people and excellent communication skills in dealing with trial subjects Strong ability to communicate and collaborate in a collegial, effective, efficient and, in particular, needs-based manner An independent, careful and structured way of working with very good time management, flexibility and agility Willingness to take on responsibility Willingness to work flexible hours and occasional full-day assignments and assignments outside the 5-day week

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