Clinical Trial Specialist (m/f) - Biopharmaceuticals

Job description

Job Description

• Support the clinical study lead in day to day business
• Set up, maintenance, filing, and archiving of the study documentation; maintenance of Trial Master File (paper and electronic)
• Interface between clinical team, CRO and any other internal or external partners in the operational study conduct
• Preparation of contracts from templates for external Service Providers and consultants
• Control and follow up of study specific invoices
• Set up and maintenance of study tracking forms
• Compilation and distribution of study materials and documents
• Tracking of study data in Clinical Trial Management Systems (CTMS)
• Organization of meetings and taking minutes
• Support clinical study lead in tracking and following up on outstanding actions from the study team meetings
• Support audits and inspections by health authorities
Position Title

Clinical Trial Specialist (m/f) - Biopharmaceuticals

Desired profile

Minimum requirements

• Min. 2 years of experience working in a clinical research environment, knowledge of the clinical trial process and GCP, experience in international clinical trials
• Excellent communication skills and proven team player in multidisciplinary, international settings
• Open minded, motivated personality with focus on details and good organizational skills
• Proficiency in all Microsoft office tools
• Fluent verbal and written English, German of advantage
Job Type

Full Time
Country

Germany
Work Location

Oberhaching (near Munich)
Functional Area

Research & Development
Division

SANDOZ
Business Unit

BioPharma SZ
Employment Type

Regular
Company/Legal Entity

Hexal AG