Summary:
For one of the most successful global players in the pharmaceutical industry DOCS is hiring a Clinical Trial Management System Specialist (m/f/d).
This role focuses on supporting the use of Merck’s Global Clinical Trial Management System and the associated business processes/data. This will require a blend of business knowledge and some technical skills.
Key responsibilities:
• Working with end users for:
- The gathering of requirements for data/report/visualization requests and ad-hoc queries
- Handling problems and errors that the end users are experiencing
- Communication of system related information
• Work with Clinical Operations users to streamline business/technical processes
• Help plan, lead and implement technology solutions to aid in automation of repetitive tasks including data cleaning activities of reference data and fulfilling data needs within the broader R&D organization
• Participate in global projects to provide innovative solutions to meet the needs of the organizational goals
Education & Experience
• Approx. 3 years of experience in the pharmaceutical industry, supporting Global Clinical Operations, and CTMS systems
• Able to work in a team setting
• Technical:
- Some database knowledge is a plus
- Experience with Microsoft Office products
- Understanding of clinical operational study data and processes
• Degree in Life Sciences (e.g. biology, chemistry, pharmaceuticals) or Technology Related Degree
Conditions:
• Full time, ideally office based in Frankfurt/Main area. Home office options can be discussed
Why this vacancy is right for you:
We offer an exciting and challenging work environment for clinical research professionals looking for an opportunity to contribute to the success of a company dedicated to researching, developing, manufacturing and marketing pharmaceuticals that improve health and quality of life.
Interested? Please submit your CV to Roger.BravoMendez@docsglobal.com or via our homepage www.docsglobal.com. We are looking forward to your application.