Clinical Research Assistant II: Study Coordination & Data

CenExel; Dubai; On-site; AED 220,000 - 257,000; Full time

Job summary

CenExel Clinical Research seeks a Research Assistant II to support Clinical Research Coordinators in achieving protocol-specific study goals while following ICH, GCP, and site guidelines. You will help manage patient charts, collect data, and liaise with participants and vendors.

The role requires clear communication, strong organizational skills, attention to detail, and the ability to react calmly in emergencies. On-site, full-time position with competitive benefits.

Qualifications

• Must be able to effectively communicate verbally and in writing.
• High school graduate or equivalent.
• May require a phlebotomy, pharmacy tech., or medical asst. certificate depending on site.
• Must have proper experience and demonstrate mastery of current position.
• Excellent computer skills and advanced knowledge of electronic equipment (i.e., e-mail, computer, fax machine, copier, etc.).
• Skilled in organization and record maintenance.
• Skilled in developing and maintaining effective working relationships with supervisors and co- workers.
• Strong personal initiative and attention to detail.
• Ability to react calmly and effectively in emergency situations.
• Ability to interpret, adapt and apply guidelines and procedures.

Responsibilities

• Creating and maintaining patient charts for all assigned studies.
• Preparing participant visits based on CRCs schedule, ensuring all source documents, assessments, lab kits and other visit materials are available and accurate. Filing of lab results, EKG results, and other communication in designated patient charts.
• Maintaining inventory of study specific supplies including lab kits, assessments and participant facing materials.
• Timely completion of data entry and query resolution for all CRFs, based on sponsor specific timelines and deadlines established in contract or other communication.
• Conducts assessments, including but not limited to, blood pressure, urine collection.
• Communicating with study participants, caregivers, third party vendors and laboratories as needed.
• Assisting Coordinators with scheduling, copying, faxing, and other clerical tasks.
• Aiding Coordinators in the facilitation of study monitoring visits.
• Completion of daily responsibilities delegated by CRC as they pertain to the study and/or participants.
• Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.

Skills

Communication

Attention to detail

Organizational skills

Education

High school diploma or equivalent

Phlebotomy/Pharmacy tech/Medical assistant certificate

Tools

Computer skills

Job description

CenExel Clinical Research seeks a Research Assistant II to support Clinical Research Coordinators in achieving protocol-specific study goals while following ICH, GCP, and site guidelines. You will help manage patient charts, collect data, and liaise with participants and vendors.

The role requires clear communication, strong organizational skills, attention to detail, and the ability to react calmly in emergencies. On-site, full-time position with competitive benefits.