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Reference: JT-897587

We are currently recruiting for a Clinical Data Analyst.

Responsibilities:
Perform CRF/eCRF data validation to ensure data integrity and quality.
Issuing data queries (DQs) manual or automated and maintenance of CRF according to DQ replies which may involve interpretation and decision making as to appropriate course of action.
Run, review, action and resolve listings of errors/inconsistencies identified by validation checks. Validate and reconcile vendor data as needed.
Reconciling the Serious Adverse Events in the CRF/eCRF and Clinical Database with the Central Safety Serious Adverse Events Database.
Participate in the QC review of study data prior to study release.
Assist with the review and evaluation of protocol against CRF.
Report findings to senior staff to assure consistency and accuracy.
Assist in the development of data validation specifications.
May serve as initial customer contact by answering basic questions from customers.
Effectively communicate w/ colleagues and customers to maintain a consistent approach in handling the work.
EDC (Inform), oncology data management, local and central lab validation experience preferred.

In addition:
Looking for Data Analyst experience, with knowledge of DM processes, but with Technical/Programming skills.

Skills we are looking for include:
InForm / Central Designer Experience
SQL
SAS
Server Administration/Web Services
Tech Writing / Validation

CK Clinical is an Equal Opportunities employer who welcomes applications from all who meet our selection criteria.

To apply for this position please send an up to date version of your CV