|Application period ends:||2017-09-29|
|Type of employment:||Permanent|
|Description of position:||
As a Clinical Data Manager you are an essential expert in our cross functional R&D study teams. Your main task is to design our clinical study databases using Medidata Rave system according to clinical study protocol (clinical phases I-IV). Your responsibilities in planning and maintaining of clinical data will include the following activities:
• Electronic Case Report Forms (eCRFs)
• Data validation and query management
• Participating in the study team activities
• Handling data from external data sources
• Data collection standardization
• Process development
• Developing and maintaining collaborative relationships with partner companies and external collaborators
|Description of unit:||
Clinical Data Management unit is part of Orion's R&D Clinical Operations organization. Clinical Operations is a key player in planning, conducting and reporting of Clinical Trials. Clinical Data Management unit consists of data managers who are responsible for activities related to database design, handling and processing of clinical data as well as process development and standardization.
We offer you a truly inspiring position in a multi-disciplinary team where open discussion about new ideas is encouraged. Your responsibilities will offer excellent opportunities to further develop your expertise. Join us – together we build well-being and do work that we are proud of!
We expect you to have experience from working with clinical studies, preferably clinical data management and at least a Bachelor's degree in a suitable field (e.g. life sciences, computer sciences, nursing). We appreciate a strong understanding of Good Clinical Practice (GCP) and knowledge of clinical study process. Basic skills in programming will be beneficial in this role and you need a fluent spoken and written English. As a person we hope that you have a strong mindset for growth and innovativeness. We value good communication and interpersonal skills. We also appreciate a positive and open attitude, willingness to learn new things and work in a continuously changing environment.
|Additional information on the position:||This position is preferably based in Espoo and you will report to the Manager of Clinical Data.|
Are you interested in knowing more about this role? Please call Riikka Raudaskoski-Tåg, Manager, Clinical Data Management 010 4263041 during the following times: Monday 25 September between 14.00 – 16.00 or Liisa Partanen, Senior Study Operations Manager, Clinical Data Management 010 426 4445 during the following times: Wednesday 20 September between 12.00-14.00.
Approved medical examination which also includes drug testing is required prior to the employment.