Clinical Research Coordinator 110161
Client of Global Medical Recruiting
Doha - Qatar
منذ 4 يوم
source : HireeJobsGulf

DohaIntroduction3 Year Contract job opportunities for international medical professionals to work in a destination which if one of the worlds next big hot spots the host country of the FIFA World Cup 2022 Qatar s premier nonprofit health care provider in Doha strives to recruit only the best international medical professionals for vacancies now available Budget Year 2019 The hospital group is the main provider of secondary tertiary healthcare in Qatar and one of the leading hospital providers in the Middle East Candidates from all countries are invited to apply The benefits outlined here are those that apply to most employees Salary offer packages are determined by the employer Global Medical Recruiting can assist the applicant with salary offer negotiations with the employer but in the end the final salary package offered is at the sole discretion of the employer and not of Global Medical Recruiting Minimum RequirementsEDUCATION Bachelor Degree in Life Sciences Bachelor Degree in Nursing Preferred Masters in Nursing Life Sciences EXPERIENCE For Bachelor in Nursing Graduate 5 years Nursing experience including 1 year research experience For BSc Graduate 3 years clinical research experience Demonstrated knowledge of International Conference on Harmonization Good Clinical Practice ICHGCP is required Preferred Experience 3 years of Clinical Research and Administrative experience LICENSE Not applicable to this post LANGUAGE SKILLS Fluent in English Oral and Written Job SpecificationPosition SummaryAs 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 Principal AccountabilitiesA Post approval regulatory process of research protocols1 Maintain confidentiality and safety of research participants at all times 2 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 research3 Plan and coordinate the initiation of research study protocol and the implementation of operating policies and procedures 4 Plan implement and maintain data collection and analysis systems in supportof research protocols and coordinate the collection and analysis of research data 5 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 6 Maintain an accurate organized and up to date research data base of all research participant appointments research data questionnaire data and research reports 7 Ensure conduct of the research according to the approved research protocol 8 Coordinate 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 9 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 proposal10 Comply with all the rules and regulations as applicable to the work assigned11 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 activities12 Primary liaison at the data collection site and responsible to explain the research protocol to potential andand active research participants including administering supervising andand ensuring an ongoing consent process 13 Demonstrate proficiency in performing research protocol related procedures as appropriate14 Complete required research function as liaison between research team and participants15 Perform other duties as may be assigned by the research team and immediate supervisor B Administrative Responsibilities1 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 2 Assist with creation of reports including annual reports progress reports project completion reports etc 3 Document all correspondence and communications pertinent to the research protocol 4 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 5 Maintain up to date participant logs appointments and tracks participants and research evaluations as appropriate to the protocol

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