Clinical Trials Coordinator: TMF & Study Support (Switzerland)

IQVIA LLC; Basel; Vor Ort; CHF 70.000 - 90.000; Vollzeit

Zusammenfassung

IQVIA LLC in Basel is seeking an experienced Clinical Trials Assistant (m/w/d) for a full-time, on-site role in Switzerland. You will support CRA and RSU teams with TMF maintenance, documentation handling, and archiving in line with SOPs.

You will coordinate CRF tracking, data flow, and communications across departments. The ideal candidate has 2–4 years in clinical research admin, solid GCP/ICH knowledge, and strong German (C1) and English skills, along with MS Office proficiency.

Qualifikationen

• Bachelor’s or higher in life science or HSD with apprenticeship in life science or pharma.
• 2–4 years of administrative support experience in clinical research roles.
• Knowledge of GCP and ICH guidelines.
• Fluent German (C1) and good command of English.
• Proficient in Microsoft Word, Excel and PowerPoint.

Aufgaben

• Assist CRAs and RSU with updating and maintaining Trial Master File (TMF).
• Prepare, handle, file, and archive clinical documentation according to SOPs.
• Coordinate tracking of CRFs, queries and data flow.
• Support on-site visits and training of new team members.

Kenntnisse

German (C1)

English proficiency

MS Office

Ausbildung

Bachelor's degree in life sciences

High School Diploma with life science apprenticeship

Tools

MS Word

Excel

PowerPoint

Jobbeschreibung

IQVIA LLC in Basel is seeking an experienced Clinical Trials Assistant (m/w/d) for a full-time, on-site role in Switzerland. You will support CRA and RSU teams with TMF maintenance, documentation handling, and archiving in line with SOPs.

You will coordinate CRF tracking, data flow, and communications across departments. The ideal candidate has 2–4 years in clinical research admin, solid GCP/ICH knowledge, and strong German (C1) and English skills, along with MS Office proficiency.