Aktuelle Jobs im Zusammenhang mit Clinical Study Coordinator - Biberach an der Riß, Baden-Württemberg - GULP – experts united


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    Biberach an der Riß, Baden-Württemberg, Deutschland GULP – experts united Vollzeit

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    Biberach an der Riß, Baden-Württemberg, Deutschland GULP – experts united Vollzeit

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    Biberach an der Riß, Baden-Württemberg, Deutschland GULP – experts united Vollzeit

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    Biberach an der Riß, Baden-Württemberg, Deutschland GULP – experts united Vollzeit

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    Biberach an der Riß, Baden-Württemberg, Deutschland GULP – experts united Vollzeit

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    vor 4 Wochen


    Biberach an der Riß, Baden-Württemberg, Deutschland GULP – experts united Vollzeit

    Unlock your career potential with GULP – experts united. We're seeking a skilled Project Assistant to join our team in the pharmaceutical industry.About the RoleRecruit test subjects for clinical studies and maintain subject files and archive documents.Manage the central registration register for study participants and maintain the homepage on the...

Clinical Study Coordinator

vor 2 Monaten


Biberach an der Riß, Baden-Württemberg, Deutschland GULP – experts united Vollzeit

Are you an experienced clinical study coordinator seeking a rewarding opportunity in the healthcare sector? If you are dedicated and passionate about your work, we share the same values. At GULP – experts united, we prioritize the satisfaction of our clients and candidates when placing qualified professionals. We are currently in search of a specialist for the administration of clinical trial participants. Seize this chance to join our team and experience our commitment to personalized support and efficient application processing. We embrace diversity and welcome individuals with disabilities.

What we provide

Competitive salary and long-term employment stability through our group Comprehensive benefits package, including holiday and year-end bonuses Up to 30 days of annual leave Opportunities for professional development through e-learning Discounts for fitness, leisure, and wellness activities

Responsibilities

Facilitating the recruitment of participants for clinical trials Organizing and managing participant files and archival documents Maintaining the central registry for study participants Updating the project website Collaborating with the study planning team, including evaluating recruitment strategies Assisting in the preparation of documentation for ethical review Conducting statistical analysis related to clinical trials (e.g., participant statistics, recruitment data)

Qualifications

Completed vocational training in a relevant field (e.g., as a project coordinator or clinical operations staff), ideally with substantial experience in clinical trials Proficient in using computers and software applications, particularly MS Office (Outlook, Word, Excel) Strong understanding of local regulations, GCP, and documentation practices, including relevant SOPs and guidelines Fluent in German with good command of written and spoken English Excellent interpersonal skills and a friendly demeanor when interacting with study participants Strong communication and collaboration abilities in a collegial and effective manner An independent, meticulous, and organized approach to work with excellent time management skills Willingness to take on responsibilities Flexibility to work varied hours and occasional extended assignments