Research Assistant at United Arab Emirates University
Al-Ayn, أبو ظبي, United Arab Emirates -
Full Time


Start Date

Immediate

Expiry Date

28 Aug, 25

Salary

0.0

Posted On

28 May, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Good communication skills

Industry

Pharmaceuticals

Description

Job Description
Research Assistant College of Medicine and Health Sciences-UAEU - employed as full-time staff member participating in research, teaching and administrative activities. - Oversee and manage the financial and operational aspects of the research project, ensuring smooth execution and compliance with institutional and funding requirements. - Coordinate administrative and organizational tasks related to laboratory operations, including support for research, grant submissions, and publications. - Maintain effective communication with the principal investigator and team members to ensure project alignment and progress tracking. - Support the daily execution of research activities, including patient recruitment, data and sample collection, data entry and management, and compliance with protocols. - Conduct data analysis and statistical evaluations, interpret findings, and contribute to the preparation of manuscripts, reports, and grant proposals. - Participate in the design and execution of research experiments, ensuring adherence to study protocols and timelines. - Provide academic and technical guidance to postgraduate students, medical trainees, and interns; assist in educational and training activities as needed. - Develop and improve workflow processes and documentation practices, promoting efficiency and quality in research operations. - Review and revise standard operating procedures (SOPs) and internal policies; submit updates for managerial approval. - Perform and document quality control and quality assurance checks to ensure data integrity and protocol compliance. - Compile, interpret, and submit experimental data to relevant databases and supervisory personnel. - Maintain accurate electronic and written records of project activities, including inventory management of biospecimens and laboratory supplies. - Proficient in applying statistical methods for data cleaning, validation, and analysis in clinical and biomedical research. - Experienced in using statistical software such as R, SPSS, STATA, SAS, and REDCap exports for data processing and interpretation. 1. Patient Recruitment & Coordination • Identify, screen, and enroll eligible participants in accordance with study protocols and ethical guidelines. • Communicate effectively with patients, families, and clinical staff to explain study procedures and obtain informed consent. • Maintain participant engagement and follow-up according to the study schedule. 2. Project Management Support • Assist in coordinating study logistics and timelines to ensure milestones are met. • Liaise with internal teams and external collaborators to support project goals. • Participate in protocol development, study start-up activities, and regular team meetings. 3. Documentation & Regulatory Compliance • Maintain accurate and up-to-date study documentation including source documents, case report forms, and regulatory binders. • Ensure compliance with IRB requirements, ICH-GCP guidelines, and institutional policies. • Assist in preparation for audits and regulatory inspections. 4. Sample Collection & Handling • Coordinate the timely collection of biological samples in collaboration with clinical teams. • Process, label, and store biospecimens in accordance with SOPs and biosafety protocols. • Maintain detailed sample tracking and documentation systems. 5. Data Management & REDCap Oversight • Create, manage, and maintain study databases using REDCap (Research Electronic Data Capture). • Ensure accurate and timely data entry, perform regular data validation, and resolve discrepancies. • Design REDCap forms and surveys in collaboration with investigators and data managers. • Monitor data quality and generate reports for study teams and sponsors as needed. • Maintain data security and user access rights within the REDCap system.
Minimum Qualification
MD, MBBS, B.Sc. and M.Sc. degree in a relevant discipline
Preferred Qualification
As above
Expected Skills
Experience in project management, data collection, data entry, data analysis, and good communication skill (Verbal and written) Preferred Arabic Speaking Minimum 2-3 years in academic or research institution setting and/or in the relevant scientific field - Train and supervise other research staff recruited on grants, graduate and undergraduate students on all aspects molecular assay
Close Date Kindly apply before the closing date.
07/06/202

Responsibilities

Please refer the Job description for details

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