Clinical Regulatory Research Associate

CI Trials; Riverside (CA); On-site; USD 28,000 - 30,000; Full time

Benefits offered by this job

Health insurance

Dental insurance

Vision insurance

401(k)

Job summary

CenExel Clinical Research in Riverside, CA seeks a Regulatory Research Assistant to support regulatory document management for clinical trials. You will assist in maintaining submissions, SOP adherence, and communications with investigators and sponsor/CRO teams.

The role is on-site, with a Monday–Friday schedule, hourly pay between $20 and $22, and a comprehensive benefits package after 30 days of employment including health, dental, vision, and 401k.

Qualifications

• Communicate effectively in writing and verbally.
• High School diploma or equivalent required.
• Minimum of 1 year of related experience in clinical research.
• Self-directed and able to work with minimal supervision.
• Able to shift priorities in a fast-paced environment.

Responsibilities

• Complies with current protocols, site SOPs, GCPs, IRB and FDA guidelines.
• Uploads regulatory documents with RealTime eDOCs System; maintain paper binders as needed.
• Prepares, organizes and maintains regulatory and training documents.
• Tracks submissions and ensures timely filing of documents.
• Obtains CVs of external investigators and signatures for regulatory docs.
• Distributes revised study documents to staff as needed.
• Obtains necessary signatures from investigators.
• Collaborates with sponsor/CRO and trial personnel on regulatory issues.
• Keeps CenExel regulatory information current.
• Participates in team meetings and training requirements.
• Assists sponsors/CROs as needed.

Skills

Verbal & written communication

Self-directed

Adaptable

Fast-paced environment

Education

High School diploma or equivalent

Tools

RealTime eDOCs

Job description

CenExel Clinical Research in Riverside, CA seeks a Regulatory Research Assistant to support regulatory document management for clinical trials. You will assist in maintaining submissions, SOP adherence, and communications with investigators and sponsor/CRO teams.

The role is on-site, with a Monday–Friday schedule, hourly pay between $20 and $22, and a comprehensive benefits package after 30 days of employment including health, dental, vision, and 401k.