Research Assistant

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 JBR
650 E. 4500 S.
Suite 100
Salt Lake City, UT 84107, USA

Description

About Us:

Each of CenExel’s research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence comprise some of the most well respected and long-standing research facilities in the country. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology. Each of our Centers of Excellence has tremendous experience and expertise in complex early phase trials, and all our sites have in-patient capability. We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success.

Along with an exceptional work environment that promotes teamwork, positive leadership, and optimal work-life balance, CenExel Clinical Research also provides highly competitive compensation and a generous benefits package to full time employees after 30 days of employment including Health Insurance, Dental, Vision, LTD, STD, Life Ins, and 401k.

Job Summary:

With limited oversight, the Research Assistant II provides direct support to Clinical Research Coordinators in the completion of protocol-specific study goals while observing strict adherence to ICH, GCP, protocol, and site guidelines and policies.

Essential Responsibilities and Duties:

• 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.

Education/Experience/Skills:

• 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.

Working Conditions

• Indoor, Office environment.
• Essential physical requirements include sitting, typing, standing, and walking.
• Lightly active position, occasional lifting of up to 20 pounds and/or pushing carts up to 50 pounds.
• Reporting to work, as scheduled, is essential.
• On site work arrangement.

CenExel Clinical Research is an Equal Opportunity Employer. All applicants will be considered for employment without regards to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or status.

Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws.For further information, please review the Know Your Rights notice from the Department of Labor.