Clinical Trial Coordinator |Job code 20-071 (Healthcare)

Required Skills & Qualifications:

• Bachelors Health sciences / Premed preferred, in-process degree acceptable
• Basic knowledge of clinical research      
• Being able to effectively and in timely manner communicate with off-site collaborators    
• Good team worker  
• Ability/desire to talk to patients     
• Spanish verbal proficiency and basic reading/writing skills helpful
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Description of Duties

• Manages the effective operation of multiple research protocols conducted by the Oncology Research Group at the Lundquist Institute/Harbor-UCLA.  Duties will be designated by the principal investigators and includes overall coordination and facilitation of research activities, submission of protocols for regulatory approval, and protocol patient care.  Collaborates with the principal investigators, other study coordinators, and other study personnel regarding study planning, implementation, budgeting, and evaluation efforts of study coordinator team.  Assigns work to manage protocol activity and ensures compliance to all standards, policies and quality measures.  Must be able to perform phlebotomy and administration of medications.

 

 

 

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