Job Description
Conduct on-site clinical monitoring which includes: document review, ensuring accurate data recording, verifying patient data, adherence to the protocol of a clinical trial in accordance with GCP/ICH guidelines, and Excel's/sponsor's SOPs. Perform on-site visits, including site qualification, initiation, monitoring and closeout visits. Maintain all files and documentation pertaining to studies. Motivate investigators in order to achieve recruitment targets. Maintaining regular contact with study sites to ensure protocol/GCP compliance. Communicate progress of study and relevant information to Project Manager and other project team members. Complete accurate study status reports in time. Deal with CRF queries in a timely manner. Participate, if requested, in the preparation of and review of study documentation, e.g. draft protocols, draft CRFs, monitoring guidelines and elements of final report. Ensure correct archiving of files on completion of a study. Travel Requirements: The position is based in Dubai and requires travel to Iran
Requirements
Qualifications: - Medical, Pharmacy or Life Sciences degree. - MSc and PhD holders would be an added advantage. - 2-3 years prior experience as a clinical research associate - Language and communication skills: Excellent English and Farsi communication skills, both written and oral. Skills Required: - Intermediate computer skills. - Be able to work in a team. - Should have responsible and mature attitude. - Possess interpersonal skills, effective communication skills and a positive diplomatic attitude in dealing with people. Able to travel to Iran region. Ability to use own initiative and pay close attention to detail. Excellent organizational skills. Independent, responsible and self motivated.
Employment Type
- Full Time
Seniority
Details
Employment type
- Full Time
Educations
Seniority
