Clinical Research Assistant I — On-Site Trials Support

California Neuroscience Research, LLC; Los Angeles (CA); On-site; USD 28,000 - 30,000; Full time

Benefits offered by this job

Health Insurance

Dental

Vision

401k

Life Insurance

STD/LTD

Job summary

CenExel Clinical Research is hiring a Research Assistant I to provide direct support to Clinical Research Coordinators on protocol-specific goals, adhering to ICH, GCP, and site guidelines. Located on-site in Los Angeles, you will work within a team focused on quality and compliance.

Responsibilities include creating patient charts, preparing participant visits, maintaining study supplies, data entry, and coordinating scheduling and monitoring visits.

Qualifications

• Excellent computer skills and advanced knowledge of electronic equipment.
• Skilled in organization and record maintenance.
• Strong personal initiative and attention to detail.
• Ability to react calmly and effectively in emergency situations.
• Ability to clearly communicate both orally and verbally.
• Interest in and knowledge of specific study indications.

Responsibilities

• Creating and maintaining patient charts for all assigned studies.
• Preparing participant visits based on CRC's schedule with source documents and materials.
• Maintaining inventory of study-specific supplies.
• Timely completion of data entry and query resolution for CRFs.
• Assisting Coordinators in assessments and scheduling tasks.
• Communicating with study participants, caregivers, and laboratories as needed.
• Assisting Coordinators with clerical tasks and monitoring visits.
• Completion of daily responsibilities delegated by CRC.

Skills

Computer proficiency

Organization

Communication

Attention to detail

Regulatory understanding

Oral and written communication

Crisis management

Study concepts

Job description

CenExel Clinical Research is hiring a Research Assistant I to provide direct support to Clinical Research Coordinators on protocol-specific goals, adhering to ICH, GCP, and site guidelines. Located on-site in Los Angeles, you will work within a team focused on quality and compliance.

Responsibilities include creating patient charts, preparing participant visits, maintaining study supplies, data entry, and coordinating scheduling and monitoring visits.