Bilingual Research Assistant I - Clinical Trials

Cenexelresearch; Florida; Ibrido; USD 36.000 - 48.000; Tempo pieno

Vantaggi offerti da questo lavoro

Health Insurance

Dental

Vision

LTD

STD

Life Insurance

401k

Descrizione del lavoro

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

You will create and maintain patient charts, prepare participant visits, manage study materials, and assist with scheduling and communications to ensure accurate data and timely visits across CNS and early phase studies.

Competenze

• High school diploma or equivalent required.
• Excellent communication skills in English and Spanish, both written and spoken.
• Strong computer skills and familiarity with common office equipment.

Mansioni

• Create and maintain patient charts for designated studies.
• Prepare participant visits based on CRC schedules; ensure all source documents and materials are available.
• Maintain inventory of study supplies including lab kits and participant materials.
• Enter data and resolve queries for CRFs within sponsor timelines.
• Conduct assessments such as blood pressure and urine collection as needed.
• Communicate with study participants, caregivers, vendors and laboratories.
• Assist Coordinators with scheduling, copying, faxing and clerical tasks.
• Support monitoring visits and daily study tasks.

Conoscenze

Verbal and written communication

Organization

Record maintenance

Interpersonal relationships

Attention to detail

Calm in emergencies

Guideline interpretation

Clear oral/written communication

Formazione

High school graduate

Strumenti

Microsoft Office

Descrizione del lavoro

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

You will create and maintain patient charts, prepare participant visits, manage study materials, and assist with scheduling and communications to ensure accurate data and timely visits across CNS and early phase studies.