# Clinical Research Monitor at Sidra Medicine

Sidra Medicine is hiring a Clinical Research Monitor. Level rates it Little AI ●○○○; you can [apply on Level](https://jobsbylevel.com/go/6121fd89-975f-48dc-b993-d2e045399d40).

AI Level 1, AI centrality 0 out of 100. Qatar.

## Details

- Company: [Sidra Medicine](https://jobsbylevel.com/companies/sidra-medicine)
- AI level: AI Level 1 (score 0 out of 100)
- Location: Qatar
- Posted: October 11, 2026
- Apply: https://jobsbylevel.com/go/6121fd89-975f-48dc-b993-d2e045399d40

## Description

JOB SUMMARY The ​ Clinical Research Monitor ​ ensures compliance of the clinical research with the currently approved protocol/amendment(s), with all applicable regulatory policies and guidelines, including Good Clinical Practice (GCP), as well as with Sidra’s policies and procedures. S/he assists in the design, development, implementation, and conduct of an effective monitoring program in accordance with GCP, institutional policies and procedures, and research protocols. As such, the clinical research monitor performs a quality control measure to ensure the integrity of research data and protection of the rights and well-being of study participants. The ​ Clinical Research Monitor ​ should monitor all study related procedures and documentation such as Informed Consent Form, Source Documentation and CRF review, Adverse Events, Serious Adverse Events and Unanticipated Problems, Investigational Product (IP) (if applicable), Laboratory and Specimen Management, Protocol Deviations/Violations, Investigator Site File (ISF) / Study binder, Roles and Responsibilities of site staff, Facilities appropriate to study execution and Enrollment target, recruitment strategies The ​ Clinical Research Monitor ​ ensures that, for those clinical research studies assigned for monitoring, the appropriate and required monitoring tasks and related activities occur as outlined in the monitoring plan or as per the procedure “Monitoring for clinical research and clinical trials” and in compliance with all related regulatory standards. S/he monitors if the reported study data is accurate, complete, and verifiable from source documents, and captures all inconsistencies observed during the clinical research studies in order to prevent recurrence on non-compliance with established regulatory standards. The ​ Clinical Research Monitor ​ is responsible for multiple projects at a time, and must have strong time management skills in addition to working both independently and in a team environment. KEY ROLE ACCOUNTABILITIES Ensures that the Investigator and study team follow the approved protocol and all approved amendment(s), if any, and adhere to current regulations, applicable ICH/GCP guidelines, local policies and standard operating procedures, including Monitoring standards and guidelines. Ensures that the investigator and the investigator's study team are performing the specified study functions, in accordance with any other written agreement between the sponsor and the investigator, and have not delegated these functions to unauthorized individuals. Adheres to the protocols’ Monitoring Plans; e.g. monitoring visit type, frequency, and required critical monitoring activities by utilizing monitoring tracking forms and other monitoring related tools and templates. Performs study conduct trainings to research teams such as Site Initiation Visits for Clinical Trials and Initial Site Trainings for Clinical Research Develops and updates Study conduct training materials as requested for researchers and study conduct templates as needed. Assists in the development and writing of clinical research monitoring plans. Conducts the monitoring visits, writes the monitoring report in details by summing up the findings of the monitoring process and put the corrective/prevention action plan for these findings. The CRM then reports to the next in line authority for approval. Issues the letter to the principal investigator and follows up with the PI to close the findings. Verifies that the investigator has filed the current Investigator’s Brochure, all documents, and all study supplies needed to conduct the study properly in their study investigator sites files and comply with the applicable regulatory requirements. Verifies that the investigator has adequate qualifications and resources documented in their study investigator sites files and remains adequate throughout the study period. Validates that the investigator and the investigator’s study team are adequately

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Source: https://jobsbylevel.com/jobs/clinical-research-monitor-at-sidra-medicine-ed2a8e

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