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Clinical Data Manager

Germany   •  Negotiable  •  Permanent, Full time


Clinical Data Manager - Munich, Germany
Very competitive salary package + Benefits
Office based

Are you looking to work for a company that looks after their employees?
Do you want to work for a company with an international presence?
Do you want to really have an impact on millions of peoples lives?
We have the role for you.

My clients global activities are growing rapidly, and they are currently seeking a full-time, office based Clinical Data Manager to join their UK Data Management team. This position will work in a team to accomplish tasks and projects that are instrumental to the companys success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.
Responsibilities:
Develop and review Data Management procedures for clinical trials with sponsor companies and other departments;
Lead the design and validation of the CRF specifications and edit checks for the electronic data capture system used for each study;
Coordinate overall Data Management by serving as primary contact for the sponsor, external data providers, and all project team members;
Interact with external data providers, and all project team members in the cross functional team; and
Attend bid defence meetings, teleconferences and face to face sponsor meetings as the lead representative from Data Management.
Qualifications & Knowledge:
Bachelors Degree in a Science or Mathematics related field with strong Data Management experience in Clinical Trials; or
Masters Degree in a Science or Mathematics related field with good Data Management experience in Clinical Trials;
Experience operating as primary contact for Data Management activities, including project oversight and direct vendor or client interaction;
Computer experience with database, spreadsheet, and EDC software (i.e. SAS, Oracle Clinical, and/or Rave preferred);
Possess an understanding of database structure and processes in data management; and
A basic knowledge of medical terminology is needed, as well as knowledge of clinical research methodologies.
My client are a full service CRO organisation providing phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. When you join my clients organisation you will be joining a team culture dedicated to supporting the development and growth of ground breaking drugs and devices. You will become part of something that will have an impact on millions of people while enjoying a competitive total compensation and benefits package and internal growth opportunities.
If you would like to know more, please apply within.

  • Agency: Cpl Life Sciences
  • Reference: JO-2204-491285
  • Posted: 25th April 2022
  • Expires: 23rd May 2022

Cpl Life Sciences

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