Scientific/Biotech

Britannia Pharmaceuticals Ltd

Clinical Research Associate - CRA Dubai

Reference: JT-896218
Job Summary:
We are urgently in need of a Clinical Research Associate - CRA.

Key Responsibilities

Ensures the integrity of clinical data and adherence to applicable regulatory, protocol and Company guidelines.
Ensures the rights, safety and wellbeing of clinical trial subjects is maintained.
In accordance with COMPANY SOPs, performs site management activities including:
site evaluation visits
site initiation visits
monitoring visits
closeout visits
Collaborates with the Core Project Team to drive subject recruitment
Establishes and maintains regular contact with Investigators, vendors and trial sites to ensure compliance with applicable regulations and the protocol.

Britannia Pharma

Clinical Data Analyst Dubai

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.

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Languages Known: English and Arabic;
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Salary & Other Benefits will be discuss during the interview.

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