Clinical Research Associate at RDI Van Nuys, CA

Comunidade Metodista; Los Angeles (CA); On-site; USD 85,000 - 110,000; Full time

Job summary

RDI is seeking a detail-oriented Clinical Research Associate to monitor trials, ensure protocol and regulatory compliance, and support site staff across multiple sites. The role emphasizes data integrity, patient safety, and collaboration with investigators in a fast-paced research environment.

Ideal candidates will have a life sciences background, 2+ years of CRA experience, strong GCP knowledge, and excellent communication skills.

Qualifications

• Bachelor's degree in life sciences, nursing, or related field; advanced degree preferred.
• Minimum 2 years of CRA or similar clinical research experience.
• Strong knowledge of Good Clinical Practice (GCP) and regulatory guidelines.
• Excellent communication and interpersonal skills.
• Ability to travel to various clinical sites as required by the study protocol.

Responsibilities

• Conduct site visits including initiation, monitoring, and closeout activities to ensure protocol compliance.
• Collaborate with investigators and site staff to train on study procedures.
• Review and verify clinical data for accuracy and completeness per GCP.
• Prepare progress reports and keep stakeholders informed about study status.
• Identify and resolve site issues, discrepancies, and non-compliance to protect study integrity.
• Assist in the selection and evaluation of study sites.
• Manage study supplies and ensure timely delivery to clinical sites.

Skills

Good Clinical Practice

Education

Bachelor's degree in life sciences or related field

Advanced degree preferred

Tools

CTMS

Job description

Clinical Research Associate job at RDI. Van Nuys, CA.

RDI is seeking a detail-oriented and motivated Clinical Research Associate (CRA) to join our dynamic team. As a leading organization in clinical research, RDI is devoted to advancing medical knowledge and contributing to the fight against diseases by conducting high-quality research studies. In this role, you will act as a critical link between the clinical sites and our research teams, ensuring that all clinical trials are conducted according to regulatory guidelines, protocols, and ethical standards. You will have the opportunity to work closely with investigators and other health professionals to monitor and evaluate study progress, data integrity, and patient safety. The ideal candidate will possess strong analytical skills and have a comprehensive understanding of Good Clinical Practice (GCP), clinical trial design, and regulatory requirements. You will be instrumental in ensuring the success of our studies by performing site selection, initiation, monitoring, and closeout visits. Join us at RDI, where you can make a meaningful impact on human health and work alongside passionate professionals committed to excellence in research. This is an exciting opportunity for those who thrive in a fast-paced environment and wish to contribute to cutting-edge clinical research.

Responsibilities

• Conduct site visits including initiation, monitoring, and closeout activities to ensure compliance with protocol and regulatory requirements.
• Collaborate with investigators and site staff to provide training on protocols and study-related procedures.
• Review and verify clinical data for accuracy and completeness in accordance with Good Clinical Practice (GCP).
• Prepare and maintain necessary documentation, including progress reports, to keep all stakeholders informed about study status.
• Identify and resolve site issues, discrepancies, and non-compliance matters promptly to ensure study integrity.
• Assist in the selection and evaluation of study sites to ensure suitability for clinical trials.
• Manage study supplies and ensure timely delivery to clinical sites, maintaining an effective inventory.

Requirements

• Bachelor's degree in life sciences, nursing, or a related field; advanced degree preferred.
• At least 2 years of experience as a Clinical Research Associate or similar role in the clinical research industry.
• Strong knowledge of Good Clinical Practice (GCP) and regulatory guidelines.
• Excellent communication, interpersonal, and presentation skills.
• Ability to travel to various clinical sites as required by the study protocol.
• Strong organizational skills and attention to detail in managing multiple priorities.
• Proficient in using clinical trial management systems (CTMS) and other relevant technologies.