Onsite Clinical Research Coordinator – Early-Phase Trials

Parexel International; Glendale (CA); On-site; USD 39,000 - 50,000; Full time

Benefits offered by this job

Health, Vision & Dental Insurance

Tuition Reimbursement

Vacation/Holiday/Sick Time

FSA/HSAs

Work/Life Balance

401(k) with Company Match

Pet Insurance

Job summary

Parexel International in Glendale, CA, is seeking a Clinical Research Coordinator to support Phase I-III trials on-site. You will partner with investigators, project managers, and study teams to ensure protocol compliance, data quality, and patient safety.

The role offers growth into CRA, project management, or leadership paths within Parexel. Candidates should have a life sciences degree and at least 2 years of clinical research experience, with knowledge of ICH-GCP and regulated environments.

Qualifications

• Bachelor's degree in Life Sciences or related field.
• Minimum of 2 years of clinical research experience as a CRC or similar role.
• Experience supporting clinical trials in a regulated environment.
• Knowledge of ICH-GCP guidelines and regulatory requirements.

Responsibilities

• Lead planning, preparation, execution, and closeout of Phase I-III trials with investigators and study teams.
• Review protocols and consent forms to ensure feasibility and compliance.
• Manage multiple active studies while maintaining timelines and patient safety.
• Identify risks, develop mitigation strategies, and escalate issues to stakeholders.
• Coordinate activities across investigators, nurses, enrollment teams, and study personnel.
• Support development and maintenance of ClinBase systems and study docs.
• Ensure data quality, query resolution, and protocol deviation assessments.

Skills

Organizational skills

Communication skills

Problem solving

Multitasking

Team collaboration

Education

Bachelor's degree in Life Sciences

Tools

EDC systems

Clinical trial databases

Job description

Parexel International in Glendale, CA, is seeking a Clinical Research Coordinator to support Phase I-III trials on-site. You will partner with investigators, project managers, and study teams to ensure protocol compliance, data quality, and patient safety.

The role offers growth into CRA, project management, or leadership paths within Parexel. Candidates should have a life sciences degree and at least 2 years of clinical research experience, with knowledge of ICH-GCP and regulated environments.