Description
Clinical Trial Specialist Office Based (Munich Pharma)
Job description:
* Support the clinical study lead in day to day business
* Set up, maintaining, filing, and archiving of the study documentation; maintenance of Trial Master File
* 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 invoices for studies and consultants
* Compilation and distribution of study materials and documents
* Organization of meetings and taking minutes thereof
* Assist clinical study lead in tracking and following up on outstanding actions from the clinical trial team meetings
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
* Fluent verbal and written English, German of advantage
For more details apply within, allow 24 hours for feedback
The recruiter has stated that all applicants for this job should be able to prove they are legally entitled to work in the EU. SRG is a trading name of Science Recruitment Group Ltd an Employment Business/Agency.
