Clinical Research Coordinator

Parexel•Glendale, CA

8d•$28 - $36•Onsite

About The Position

Parexel is seeking a Clinical Research Coordinator (CRC) to join their Early Phase Clinical Research team in Glendale, California. This is a fully on-site position where the CRC will support the planning, preparation, execution, and closeout of Phase I-III clinical trials. The role emphasizes ensuring patient safety, protocol compliance, and data quality. The CRC will collaborate with investigators, project managers, research associates, nurses, and other operational teams, playing a critical part in protocol implementation, risk identification, and study oversight. This role offers opportunities for career growth into areas like Clinical Research Associate (CRA), Project Management, or Quality/Risk Compliance.

Requirements

Bachelor's degree in Life Sciences, Health Sciences, Nursing, or a related field, or equivalent combination of education and experience.
Minimum of 2 years of clinical research experience as a Clinical Research Coordinator or related clinical research 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.

Nice To Haves

Experience within a Contract Research Organization (CRO) environment.
Experience supporting Phase I-III clinical trials.
Experience with clinical trial databases and electronic data capture systems.

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 escalate 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.