For one of our clients in Zaventem, we are currently looking for a "Clinical Data Manager".
Job Description
The Senior Clinical Data Manager will be responsible for all aspects of clinical data management associated with data cleaning and quality review processes for assigned projects with minimal supervision. S/he ensures clinical trial data collected meet the highest standards of data integrity, while meeting timelines and budgets.
Responsibilities
Support CRF design, review and validation of clinical database,
Have the ability to support a number of moderate complexity / complex trials with minimal supervision;
Be responsible for creation of data management plans and other data management documentation as needed with minimal oversight;
Monitor progress and conduct of their respective projects, including all data cleaning and QC activities to ensure all remain on target to project timelines;
Be responsible for coordinating, facilitating and participating in all data management activities from initiation of protocol through database lock with minimal oversight, partnering as appropriate with Clinical Operations, Franchise and other BSDM functions for their respective projects;
Be responsible for participating in ongoing data review throughout the conduct of the study, including being responsible for the correction of errors and discrepancies management for the life of a project;
Proactively identify and address issues that may impact the quality of the data, deliverables or timelines;
Be responsible for handling of non-CRF data, including lab data and image handling;
Be responsible for coordinating with Medical Affairs organization to facilitate data coding and safety reviews as needed;
Contribute towards process improvement, data standards and efficiency gaining initiatives within data management working with data management leadership as needed;
Be responsible for ensuring all clinical data management documentation is stored and archived in a timely and compliant manner;
Know and follow all regulations that apply to the job, and maintain the highest levels of professionalism, ethics and compliance at all times;
Performs other related duties as required.
Do the above responsibilities fit you like a glove?
Upload your CV and motivation letter via the "apply now" button and you can expect feedback from us soon.
If something is not entirely clear, you can reach out to us by telephone of course.
Requirements
Therapeutic area knowledge in at least one of orthopedics, gynecology, cardiovascular, or general surgery preferred
Proficient in computer technology used in an office environment (Microsoft Word, Excel, etc).
Strong verbal and written communication skills.
Knowledge of GCP and regulatory requirements regarding clinical data management documentation and software.
Experience with Electronic Data Capture (EDC), Medidata RAVE preferred.
Knowledge of medical terminology and use of coding dictionaries (MedDRA, WHO Drug).
A Bachelor's degree (or equivalent) in the biological sciences, Computer Science or related discipline, with at least 4 years of clinical data management experience in Medical Device or Pharmaceuticals
Experience of supporting trials with minimal supervision.
Benefits
A balanced salary package based on your capabilities and experience.
Existing right to work in Europe required ( please read job spec in full before applying ).
Vacancy Number: 16752
