Hiring Clinical Research Assistant

- Salary = 6 K AED Per Month

- Location- Abu Dhabi

JD as follows:

- develop and write trial protocols (outlining purpose and methodology)

- present trial protocols to a steering committee

- design data collection forms, known as case report forms (CRFs)

- coordinate with the ethics committee, which safeguards the rights, safety and wellbeing of all trial subjects

- manage regulatory authority applications and approvals that oversee the research and marketing of new and existing drugs

- identify and assess the suitability of facilities to use as the clinical trial site

- identify/select an investigator who will be responsible for conducting the trial at the trial site

- liaise with doctors, consultants or investigators on conducting the trial

- set up the trial sites - ensuring each centre has the trial materials, including the trial drug often known as the investigational medicinal product (IMP)

- train the site staff to trial-specific industry standards

- monitor the trial throughout its duration, which involves visiting the trial sites on a regular basis and dealing with and solving any issues

- verify that data entered on to the CRFs is consistent with patient clinical notes, known as source data/document verification (SDV)

- collect completed CRFs from hospitals and general practices

- write visit reports and file and collate trial documentation and reports

- meet with team members to discuss on-going trials, results and any trends or adverse events

- ensure all unused trial supplies are accounted for

- close down trial sites on completion of the trial

- discuss results with a medical statistician, who writes technical trial reports

- archive study documentation and correspondence

- prepare final reports and occasionally manuscripts for publication