Clinical Data Manager (all genders) with Japanese, EU Based

Location
Europe
Salary
Competitive
Posted
08 Feb 2021
Closes
10 Mar 2021
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

Linical Co., Ltd. (‘Linical’) is a premier global CRO headquartered in Osaka, Japan, listed in the prime segment of the Tokyo Stock exchange, and dedicated to serve its clients as a true partner in development. With more than 700 employees Linical directly covers a total of more than 20 countries in Europe, North America and Asia-Pacific including Japan via its own offices and staff.

Linical’s European arm is headquartered in Frankfurt, Germany with a substantial presence in Paris and Madrid. Its geographic footprint facilitates a significant presence in the leading Western European markets, combined with well-established affiliate operations in key emerging markets in Central- and Eastern Europe.

We offer individualized solutions that are tailored to the specific needs of our sponsors. We work as integrated teams functioning with maximum transparency throughout each study, making sure that the sponsor is kept up to date on all study parameters and progress. We are dedicated to the highest standards of quality, with a special focus on the therapeutic areas oncology, immunology and CNS, based on experience and expertise.

At Linical, we embrace the opportunities and possibilities that are held by diversity, equal opportunity and inclusion. We value bringing together individuals from diverse backgrounds regardless of race, disability, ethnicity, gender, sexual orientation or any other legally protected characteristic. Linical will consider all candidates that match with the requirements of the position, promoting diversity and equal opportunity for all.

Description of the tasks / routine work:

• CRF design, Production of the DMP & writing of the edit checks specifications
• Review of draft protocols and CRF’s for consistency and accuracy. Review CRF design where appropriated.
• Set-up and maintenance of the Project Binder and all related documentation.
• Review the annotated CRFs.
• Testing of clinical study database.
• Testing of edit checks and data listings.
• Co-ordinate and oversee the testing of the database structure and edit check programs.
• Support clinical data programmer with programming activities and database setup.
• Defining electronic data transfer specifications. Liaison with contract laboratories and other providers of electronic data to co-ordinate the receipt ensuring that it is complete, consistent, in the required format and received in a timely manner in order for project timelines to be met.
• Be involved in the processing of clinical data including CRF review, query generation and resolution, review of electronic data, medical coding and quality control procedures.
• Generation of project status reports, and provides them to the corresponding project manager.
• Liaising with the project team members and the Data Project Manager to ensure that the status of the study and the goals and timelines are fully understood by all.
• Closing and locking of the databases and all activities related to the final cleaning of the data in preparation for lock including direct contact with sites to resolve outstanding queries.
• To be able to perform all the tasks described previously by themselves.
• Any other task requested by line manager.

Qualifications: 

Very High level or Native Level of JAPANESE. 

Disciplined Work Approach, Communication, Problem Solving, Attention to Detail, Computer Skills, Language Skills.

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