Clinical Research Coordinator

W2 or 1099! NEURO CRC needed

Job Title: Clinical Research Coordinator

Company Overview: is a leading clinical research organization dedicated to advancing healthcare through innovative research and development. We specialize in conducting clinical trials across various therapeutic areas, collaborating with healthcare providers, sponsors, and patients to bring cutting-edge treatments to market.

Position Summary: We are seeking a highly motivated and detail-oriented Clinical Research Coordinator to join our dynamic team. The Clinical Research Coordinator will be responsible for supporting the planning, implementation, and coordination of clinical trials conducted within our site network. This role offers the opportunity to contribute to groundbreaking research and make a meaningful impact on patient care.

Key Responsibilities:

• Coordinate and oversee all aspects of clinical trials in accordance with protocol requirements, regulatory standards, and Good Clinical Practice (GCP) guidelines.
• Serve as the primary point of contact for investigators, study sponsors, and research team members to ensure effective communication and collaboration throughout the trial process.
• Facilitate study startup activities, including protocol development, regulatory submissions, and study site selection.
• Screen and recruit eligible participants for clinical trials, ensuring informed consent and compliance with study protocols.
• Conduct study visits, collect and manage study data, and maintain accurate and complete study documentation.
• Monitor participant safety and protocol adherence, promptly report adverse events, and implement corrective actions as needed.
• Coordinate study-related activities with external vendors, including laboratories, imaging facilities, and central review boards.
• Assist with study budget management, tracking expenses, and ensuring adherence to financial guidelines.
• Contribute to study progress reports, presentations, and publications as required.
• Stay current with industry trends, regulatory updates, and best practices in clinical research.

Qualifications:

• Bachelor's degree in a scientific or healthcare-related field; relevant certifications (e.g., CCRC, ACRP, SOCRA) preferred.
• Minimum of [insert number] years of experience in clinical research coordination or related role, preferably in a clinical trial site or research organization.
• Strong understanding of clinical trial conduct, protocol development, and regulatory requirements (FDA, ICH, etc.).
• Proficiency in electronic data capture systems, EMR/EHR platforms, and Microsoft Office Suite.
• Excellent communication, interpersonal, and organizational skills, with the ability to work effectively in a multidisciplinary team environment.
• Detail-oriented with a high degree of accuracy and the ability to prioritize tasks and meet deadlines.
• Flexibility to adapt to changing priorities and work independently with minimal supervision.
• Commitment to ethical conduct, patient safety, and data integrity in clinical research.

Location: Southern California