Minimum Requirements

ESSENTIAL EDUCATION & EXPERIENCE: 

For - Bachelor in Nursing (Graduate): 5 years Nursing experience including 1 year research experience.

For - BSc Degree (Graduate): 3 years clinical research experience, demonstrated knowledge of International Conference on Harmonization – Good Clinical Practice (ICH-GCP) is required.

MEDICAL LICENSE:

Not applicable. 

MEDICAL LICENSE:

Fluent in English. 

Specification

POSITION SUMMARY:

As an Academic Health System the Corporation would like to employ staff who contribute to the mission and vision of the Corporation. Research is a key and integral component to this vision and the post holder must be able to contribute to an Integrated strategic vision and planning for Clinical, Research and Education and training.

The Clinical Research Coordinator (CRC), under supervision of the Principal Investigator (PI), will coordinate clinical research studies in accordance with international Good Clinical Practice and Good Research Practices guidelines. A successful candidate would The Clinical Research Coordinator will assist with completion and submission of all research documents, the preparation of study related correspondence, perform data entry, maintain research files, procure study supplies, route procurement requests, ensure budget adherence and perform other administrative support tasks related to the research protocol.

The post holder will also be required to lead on and undertake educational and training programs.

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 communicate effectively with the PI / Research Team leader and other site personnel, research participants, and with research sponsors as appropriate to the research proposal

Comply with all the rules and regulations as applicable to the work assigned

Create and adhere to a data quality and quality assurance plan appropriate to the research protocol including participating in Data safety and monitoring (DSM) and Quality and patient safety (QPS) activities

Primary liaison at the data collection site and responsible to explain the research protocol to potential andand active research participants, including administering, supervising and ensuring an ongoing consent process.

Demonstrate proficiency in performing research protocol related procedures as appropriate

Complete required research function as liaison between research team and participants

Perform other duties as may be assigned by the research team and immediate supervisor.       

Administrative Responsibilities

Maintain and update all documentation for IACUC, Biosafety and IRB (including protocols, approvals, amendments, modifications, revisions)as well as any communications with the research sponsor and regulatory agency/ies as appropriate, for issues including but not limited toprior approvals, change in scope, enrollment logs.

Assist with creation of reports, including annual reports, progress reports, project completion reports etc...

Document all correspondence and communications pertinent to the research protocol.

Organize and facilitate meetings, conferences and other events associated with research activities and may perform and coordinate outreach and educational activities, as appropriate to research proposal objectives with notes and feedback of specific participant and family questions. Ensures completion of all items discussed and maintains minutes during such meetings.

Maintain up to date participant logs, appointments and tracks participants and research evaluations as appropriate to the protocol

Financial Management:

Preparation and assisting with audit report trails of project budget expenditures

Accountability:

Responsible for maintaining accuracy, timeliness and quality of research reports and data related to research projects

Effective and timely communications of research with research team, MRC, DSMB, other research coordinators etc...

Is compliant with applicable IRB/ IACUC/IBC/RSAC committee regulations while implementing protocols. 4. The post holder will be required to adhere to research legislative and regulatory requirements including HMC and SCH policies, Food and Drug Administration (FDA) Good Clinical Practice (GCP) and International Conference on Harmonization – Good Clinical Practice (ICH-GCP).

About the Employer

WORK AT QATAR'S LEADING PUBLIC HEALTHCARE PROVIDER:

The healthcare provider to over two million expatriates and Qatari nationals living and working in Qatar.

This is a diverse and exciting organization where over 90 different nationalities work together for the single purpose of improving the quality of human life through patient care, education and research.

The organization is committed to developing of employees through training, educating and career advancement opportunities.

You will be constantly learning. Your ideas will be welcomed in an atmosphere of collaboration and teamwork. Your individuality will be recognized. 

You are invited to apply for job openings. 

MORE ABOUT QATAR:

Qatar is home to many expats who relocated here for work and those drawn to its life of luxury, this is most evident in the capital city Doha.

Doha is located on the coast of the Persian Gulf in the east of Qatar. Doha has awesome attractions.

You will be able to experience adventure, buzzing nightlife, culture or relaxation.

Qatar does not only offer the most amazing desert landscapes but also stunning beautiful beaches to enjoy.