Clinical Research Associate

Job Summary:

We are seeking The Clinical Trial oversees and manages the execution of clinical trials, ensuring compliance with regulatory standards, timelines, and quality metrics.

This role involves cross-functional leadership, strategic planning, and direct supervision of study teams to deliver successful trial outcomes.

Key Responsibilities:

• Provide mentorship and guidance to team members, fostering a culture of accountability, innovation, and continuous improvement.
• Monitor process performance, identifying and addressing risks, issues, and deviations to maintain service excellence.
• Oversee client onboarding, workflow management, quality assurance, and process optimization to ensure compliance with industry standards and client expectations.
• Prepare and present operational reports, performance updates, and insights to senior management and stakeholders.
• Serve as the primary point of contact for clients, ensuring professional and courteous communication.
• Maintain strong client relationships by providing clear, accurate, and proactive support to meet business objectives.

Areas of Expertise:

• Medical Record Interpretation: Proficient in analyzing various components of medical records, with strong understanding of confidentiality standards and data security protocols for research subjects.

• Medical Terminology & Clinical Knowledge: Solid foundation in medical terminology, anatomy, and physiology through formal coursework and hands-on experience in clinical and research environments.

• Oncology Research Experience: Prior experience working in oncology-focused research settings, contributing to clinical trials and patient data management.

• Electronic Medical Records (EMR) & Clinical Systems: Extensive knowledge of EMR platforms such as Power Chart, and expertise in using clinical trial management systems like OnCore, along with other specialized data entry tools