Coordinator - Clinical Research I - FT - Days - OHR

Responsibilities

• Manages the handling of adverse events, compliance and other participant-related issues.
• Handles resolution of data queries with sponsor.
• Completes, organizes, and submits Institutional Review Board (IRB) for phase 1 - 4 trials required by the sponsor.
• Conducts initiation, monitoring and close out visits with the sponsor.
• Collaborates to ensure compliance with local, state and federal regulations and standards.
• Assists with responding to and preparing for audits and participates in audits.
• Processes and ships research specimens per protocol guidelines.

Competencies

• ACCOUNTABILITY
• ACCURACY
• Clinical Research - Regulatory Compliance
• CUSTOMER SERVICE
• DEVELOPS RELATIONSHIPS
• EFFECTIVE COMMUNICATION
• PATIENT AND FAMILY CENTERED CARE
• RESEARCH - REPORTING - COORD
• RESPONDING TO CHANGE
• STANDARDS OF BEHAVIOR

Education And Certification Requirements

A high school diploma or equivalent is required.

Additional Job Information

Complexity of Work: Requires critical thinking skills, effective communication skills, decisive judgment and the ability to work with minimal supervision. Demonstrates ability to work effectively as a team member. Ability to multi-task.

Working Conditions And Physical Requirements

Keyboard Entry: 80%

Shift Days

Employment is subject to post offer, pre-placement assessment, including drug testing. If you need reasonable accommodation during the application process, please call 954-276-8340 (M-F, 8am-5pm) or email TalentAcquisitionCenter@mhs.net