Clinical Research Assistant II - Impactful Trials Support

CenExel JBR; Dubai; On-site; AED 154,000 - 228,000; Full time

Benefits offered by this job

Health Insurance

Dental

Vision

401k

Life Insurance

Job summary

CenExel Clinical Research is seeking a Research Assistant II to provide direct support to Clinical Research Coordinators in completing protocol-specific study goals, while adhering to ICH, GCP, protocol, and site guidelines.

The role involves creating patient charts, preparing visits, maintaining study materials, and data entry within an on-site office environment. Strong communication, organization, and a detail-oriented approach are essential.

Qualifications

• Must be able to effectively communicate verbally and in writing.
• High school graduate or equivalent.
• Phlebotomy, pharmacy tech., or medical assistant certificate may be required depending on site.
• Experience and mastery of current position expected.
• Strong computer skills and familiarity with office equipment.

Responsibilities

• Create and maintain patient charts for all studies.
• Prepare participant visits based on CRC schedule and ensure all documents and materials are available.
• Maintain inventory of study supplies including lab kits and materials.
• Complete data entry and resolve CRF queries per sponsor timelines.
• Conduct assessments such as blood pressure and urine collection.
• Communicate with study participants, caregivers, vendors and laboratories.
• Assist Coordinators with scheduling, copying, faxing, and clerical tasks.
• Aid Coordinators in study monitoring visits.
• Perform daily duties as delegated by CRC.

Skills

Verbal & written communication

Computer skills

Organization & record keeping

Attention to detail

Guidelines interpretation

Education

High school diploma or equivalent

Job description

CenExel Clinical Research is seeking a Research Assistant II to provide direct support to Clinical Research Coordinators in completing protocol-specific study goals, while adhering to ICH, GCP, protocol, and site guidelines.

The role involves creating patient charts, preparing visits, maintaining study materials, and data entry within an on-site office environment. Strong communication, organization, and a detail-oriented approach are essential.