Onsite Clinical Research Coordinator — Phase I-III Trials

Parexel; Glendale (CA); On-site; USD 80,231,000 - 103,155,000; Full time

Benefits offered by this job

Health, Vision & Dental Insurance

Tuition Reimbursement

Vacation/Holiday/Sick Time

401(k) with Company Match

Pet Insurance

Job summary

Parexel in Glendale, CA seeking a Clinical Research Coordinator to join the Early Phase Clinical Research team on-site. You will support planning, execution, and closeout of Phase I-III trials, ensuring patient safety and data quality.

The role collaborates with investigators, nurses, and project managers, with opportunities for career growth into CRA, project management, or leadership positions. Weekend study support may be required.

Qualifications

• Bachelor's degree in Life Sciences, Health Sciences, Nursing, or related field.
• Minimum of 2 years clinical research experience as a Clinical Research Coordinator or related role.
• Experience supporting clinical trials and study operations in a regulated environment.
• Knowledge of ICH-GCP guidelines, regulatory requirements, and clinical trial processes.
• Strong verbal and written communication skills.
• Proven ability to prioritize workload, manage competing deadlines, and work effectively within cross-functional teams.
• Ability to work fully onsite and support weekend study activities when required.

Responsibilities

• Lead the planning, preparation, execution, and closeout of Phase I-III clinical trials in collaboration with investigators, project managers, and study teams.
• Review study protocols, informed consent forms, and study materials to ensure operational feasibility and compliance.
• Manage multiple active studies simultaneously while maintaining quality, timelines, and patient safety standards.
• Identify protocol or operational risks, develop mitigation strategies, and upscale issues proactively to stakeholders.
• Coordinate study activities across investigators, research associates, nurses, enrollment teams, project managers, and laboratory personnel.
• Support the development, setup, and maintenance of ClinBase systems and study-specific documentation.
• Oversee study data quality, query resolution, protocol deviation assessments, and documentation compliance.
• Assist with study-specific training and ensure operational teams are prepared to execute protocol requirements.
• Ensure all clinical trial activities are performed in accordance with ICH-GCP guidelines, regulatory requirements, and Parexel SOPs.
• Contribute to a collaborative and supportive team environment while delivering high-quality results for sponsors and patients.

Skills

Organizational skills

Communication

Problem-solving

Multi-priority management

Education

Bachelor's degree in Life Sciences/Health Sciences/Nursing or related field

Tools

EDC systems

Clinical trial databases

Regulatory knowledge

Job description

Parexel in Glendale, CA seeking a Clinical Research Coordinator to join the Early Phase Clinical Research team on-site. You will support planning, execution, and closeout of Phase I-III trials, ensuring patient safety and data quality.

The role collaborates with investigators, nurses, and project managers, with opportunities for career growth into CRA, project management, or leadership positions. Weekend study support may be required.