The Clinical Data Analyst II (CDA II) shall be responsible for data processing activities on a project and shall ensure quality standards according to SOPs and ICH-GCP. Areas of responsibility shall include; data cleaning and query generation, support in data entry and CRF tracking, medical coding,
SAE reconciliation and quality support on projects The CDA shall support on project meetings and telephone conferences where required. The CDA shall support the Project Lead on a project on tasks as needed.

Qualifications :
•At least 3 years experience in a similar DM role within clinical research environment.
•Experience in using any EDC system or SAS is preferred.
Tertiary qualification is essential.