Responsibilities include;
- Liaising and collaboration with the director, data management team, and sponsor with regards to all aspects of the data management projects
- Contribute to the revision and improvement of the SOPs
- Review SAS listings and tables
- Complete data validation and data cleaning activities
- Reconciliation of data from external sources such as SAE, IVRS and central laboratory
Creation and review of CRF and eCRF
Requirements;
- BSc in Life Science subject with 3-5 years of data management experience
- Experience working in a CRO, Pharmaceutical or Biotechnology
- Proficient in SAS
