Clinical Research Coordinator 259097

Medix™; Anaheim (CA); Sur place; USD 55 000 - 75 000; Plein temps

Résumé du poste

Medix seeks a Clinical Research Coordinator to assist with coordinating patient involvement from study initiation to completion. You will organize research information, observe subjects, collect data, and support data analysis and reporting.

You will document adverse events, deviations, and other issues, maintain quality and compliance, and support regulatory duties. You will engage in protocol development, ensure sponsor communications, educate participants, and conduct safety assessments as

Qualifications

• Coordinating clinical study activities
• Experience with data collection and management
• Attention to regulatory requirements
• Communication and collaboration skills
• Strong organizational abilities
• Familiarity with adverse event reporting
• Analytical mindset for data review
• Ability to educate participants and caregivers
• Experience with protocol adherence
• Ability to document and report findings
• Knowledge of source documentation and study supplies
• Willingness to perform general trial duties

Responsabilités

• Assists with coordinating all aspects of patient involvement from study initiation until study completion.
• Organizes research information for clinical trials.
• Observes subjects and assists with data analysis and reporting.
• Schedules the collection of data.
• Documents adverse events, protocol deviations, and other unanticipated problems appropriately.
• Reports research data to maintain quality and compliance.
• Performs administrative and regulatory duties related to the study as appropriate.
• Participates in other protocol development activities.
• Ensures site receives accurate information and supplies from sponsors (i.e.: source, protocol, scales, supplies, approvals, contacts, etc.)
• Educates potential participants and caregivers on protocol specific details and expectations.
• Performs safety and efficacy assessments per protocol (vital signs, EKGs, blood draws and other assessments as assigned).
• Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive

Description du poste

• Assists with coordinating all aspects of patient involvement from study initiation until study completion.
• Organizes research information for clinical trials.
• Observes subjects and assists with data analysis and reporting.
• Schedules the collection of data.
• Documents adverse events, protocol deviations, and other unanticipated problems appropriately.
• Reports research data to maintain quality and compliance.
• Performs administrative and regulatory duties related to the study as appropriate.
• Participates in other protocol development activities.
• Ensures site receives accurate information and supplies from sponsors (i.e.: source, protocol, scales, supplies, approvals, contacts, etc.)
• Educates potential participants and caregivers on protocol specific details and expectations.
• Performs safety and efficacy assessments per protocol (vital signs, EKGs, blood draws and other assessments as assigned).
• Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive