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Clinical Research Coordinator
3 weeks ago
**JOB PURPOSE**:
Clinical Research Coordinators are tasked with administering clinical trials. Their primary responsibilities include managing clinical trials and collecting data, informing participants about study objectives, and administering questionnaires.
**KEY RESPONSIBILITIES AND TASKS**
- Adhere to Good Clinical Practices and the study protocols
- Ensure scientific integrity of data and protect the rights, safety, and well-being of patients enrolled in clinical trials
- Provide patient with written communication of their participation (i.e. copy of the signed informed consent)
- Meet with patient for each visit and maintain accessibility to discuss any questions/concerns regarding the study
- Package and ship blood/urine specimens at scheduled patient visits
- Schedule all patient research visits and procedures consistent with protocol requirements
- Complete and maintain case report forms, and review them against the patient’s medical record for completeness and accuracy
- Administer questionnaires/diaries/other patient material per protocol
- Ensure that non-serious and serious adverse events are properly documented and reported
- Screen all laboratory results when received and follow protocol procedure regarding abnormal results
- Manage communication with study vendors (lab assessments vendors, imaging vendors, etc) as needed
- Ensure the filing and maintenance of all study documents
- Schedule monitor visits and set up for monitoring visits prior to monitor’s arrival
- Act as a liaison between site staff and different departments
**Job Types**: Part-time, Temporary
Contract length: 6 months
Ability to commute/relocate:
- Manama: Reliably commute or planning to relocate before starting work (required)
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