Clinical Research Coordinator (onsite)

Job Summary

Role Responsibilities:

• Coordinate clinical research studies and maintain a safe study environment according to health and safety policies under the direction and delegation of the Principal Investigator

• Safeguard the well-being of subjects act as a volunteer advocate and address subjects concerns while ensuring the highest quality-of-care practices

• Maintain up-to-date study protocols case report forms (CRFs) Electronic Data Capture (EDC) systems and other study documents

• Plan and coordinate logistical activity for study procedures according to the study protocol

• Perform clinical set-up and preparation for the study including labeling specimen collection tubes and containers inventory of required supplies and setting up or troubleshooting equipment and/or study issues

• Assist with data entry data quality checking and query resolution to ensure adherence to study protocol and quality control for content accuracy and completeness

• Assist in study enrollment by recruiting screening and orienting volunteers according to the study protocol

• Correct custody of study drug according to site standard operating procedures

• Perform a variety of complex clinical procedures on subjects including but not limited to vital signs phlebotomy etc.

• Collect record and report clinical data and findings appropriately in CRFs while collaborating with study investigator about study-related adverse events and serious adverse events according to the study protocol.

Qualifications

• Bachelors Degree

• Actual onsite experience (2-3 years)

• Working knowledge of clinical trials

• Working knowledge of the principles of Good Clinical Practices (GCP)

• In-depth knowledge of departmental protocol and study-specific operating procedures consent forms and study schedules

• Skill in carrying out required clinical procedures such as intravenous catheter insertion and spirometry testing

• Good skill in using MS Windows and Office applications such as Access Outlook and Word
  

IQVIA is a leading global provider of clinical research services commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements misrepresentations or material omissions during the recruitment process will result in immediate disqualification of your application or termination of employment if discovered later in accordance with applicable law. We appreciate your honesty and professionalism.

Required Experience:

IC

Key Skills

• Experience Working With Students
• Google Docs
• Organizational skills
• Classroom Experience
• Data Collection
• Materials Handling
• Workers' Compensation Law
• OSHA
• Special Operations
• Team Management
• Experience with Children
• Supervising Experience

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