Clinical Research Assistant I — Clinical Trials Support

CenExel; Los Angeles (CA); On-site; USD 42,000 - 45,000; Full time

Job summary

CenExel Clinical Research is seeking a detail-oriented individual to provide direct support to Clinical Research Coordinators in achieving protocol-specific study goals, while strictly following ICH, GCP, protocol, and site guidelines. The role includes creating patient charts, coordinating participant visits, and maintaining study materials.

The position involves data entry, inventory management, and assisting with monitoring visits in a collaborative, office-based setting.

Qualifications

• Interest in and knowledge of specific study indications.
• Excellent computer skills and advanced knowledge of electronic equipment.
• 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.
• Ability to clearly communicate both orally and verbally.

Responsibilities

• Creating and maintaining patient charts for all assigned studies.
• Preparing participant visits based on CRC's 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.
• Assisting Coordinators in 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.

Skills

Computer skills

Organization

Communication

Attention to detail

Teamwork

Emergency response

Guideline interpretation

Data entry

Job description

CenExel Clinical Research is seeking a detail-oriented individual to provide direct support to Clinical Research Coordinators in achieving protocol-specific study goals, while strictly following ICH, GCP, protocol, and site guidelines. The role includes creating patient charts, coordinating participant visits, and maintaining study materials.

The position involves data entry, inventory management, and assisting with monitoring visits in a collaborative, office-based setting.