1 Clinical Trials jobs in Qatar

**Overseas Contract Jobs - Doha Qatar**

**Clinical Research Officer II - Grade 110**

**Designation: IRB Research Monitor**

The post holder main focus will be on monitoring research studies and their adherence to the ethical conduct, as outlined by the research protocol and as per the IRB approval.

In order to be considered for this vacancies you need to meet the essential education and experience requirements as mentioned below under "Minimum Requirements".
- Global Medical Recruiting (GMR) is a "Registered Recruitment Partner" with the Medical Group in Qatar. _GMR does not charge you (the applicant) any recruitment fees as we are paid by the Medical Group for our placement services._
- Package
- Minimum Requirement
- Job Specification
- About the Employer

**Package**:
**OVERSEAS CONTRACT**:
**Basic Salary: +/- 10 850 QAR per month. **This is an **estimated amount. The **offered amount is the discretion of the employer.**

**Transport Allowance: 1250 QAR per month.**

**Accommodation**: Provided.

**Annual Leave**: 40 calendar days.

**Air Passage Entitlement**: Economy class air passage/flight ticket for self and family - up to 3 children up to 18 years old, on joining, annual leave & repatriation (provided that he/she obtained residence permit for them under his/her sponsorship).

**Baggage Allowance**: Unaccompanied baggage for yourself - up to 50 kg and family up to 200 kg on joining, and 100kg for self and 250 kg for family on repatriation, to be reimbursed at standard rate.

**PLEASE ENSURE THAT YOU MEET THE MINIMUM REQUIREMENTS BEFORE APPLYING** View Minimum Requirements**Minimum Requirements**:
**ESSENTIAL EDUCATION**:
Bachelor in healthcare related field, science engineering or clinical research.

**ESSENTIAL EXPERIENCE**:
3 years of experience with minimum of 2 years in research related field (either as part of educational programs, or during professional employment) for Graduates with healthcare related degrees or Clinical Research Management

3 years of research experience (this could be in clinical, academic, pharmaceutical or healthcare related industry) for Graduates with science or engineering degrees.

**MEDICAL LICENSE**:
Not applicable.

**LANGUAGE**:
Fluent in English.

**Specification**:
***:
**Main accountabilities**:
Monitoring of research studies approved by MRC/IRB, providing support to research team for study conduct.

Interacting and communicating effectively with the Principal Investigator (PI)/Research team leader and other research personnel as required by the research project

Review the progress reports and supporting documents for further IRB review

Coordinating and managing the activities of sites to ensure compliance with study protocol requirements

To conduct monitoring of the study at the investigator site in accordance with ICH-GCP guidelines on clinical trial monitoring and local regulatory requirements

Ensure the delivery of appropriate quality improvement training for investigators and key study personnel during the monitoring visit.

**Must have**:

- Full understanding of the IRB Monitoring Policy and Human Research Program Policies in addition to ICH-GCP and MoPH regulations.
- Ability to review source documents, Case report forms, Informed consent forms and other research documents for compliance.
- Ability to conduct study initiation/Monitoring/Auditing Visits to study sites as directed by the IRB to ensure adherence to protocol, accurate data collection via comprehensive source document verification, and investigational product/biological samples/supplies accountability

**RESPONSIBILITIES**:
**_ Post approval regulatory process of research protocols_**

Maintain confidentiality and safety of research participants at all times.

Adhere to Good Clinical Practice (GCP), Good Laboratory Practice (GLP), Good Research practices (GRP), infection control practices and other mandated requirements to ensure safe and effective conduct of research

Plan and coordinate the initiation of research study protocol and the implementation of operating policies and procedures.

Plan, implement and maintain data collection and analysis systems in support
of research protocols and coordinate the collection and analysis of research data.

Recruit instruct and coordinate the appointment and evaluation of research participants and /or volunteers as appropriate to the specific objectives and work scope of the research protocol.

Maintain an accurate, organized and up to date research data base of all research participant appointments, research data, questionnaire data and research reports.

Ensure conduct of the research according to the approved research protocol.

Co-ordinate the day to day activities of technical support staff specifically engaged in the carrying out of the clinical research protocol, appropriate to the position and perform work of the research protocol as assigned by the PI / team leader, in accordance with the specific proposal objectives.

Interact and co