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Senior Clinical Data Coord(China-BJ/SH/DL) - (1603363) in Shanghai, CN at IQVIA™

Date Posted: 4/11/2018

Job Snapshot

Job Description

Join us on our exciting journey!

IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward.
The world's leading pharmaceutical services organization is powering the next generation of healthcare.  If you want to make a difference in global healthcare,  IQVIA™ is the place for you. You'll be connected with an organization that is changing the way drugs are developed, profiled and marketed. More than 19,000 people throughout the world have already chosen to join IQVIA™. 

 
Of the world's top 30 best-selling drugs, IQVIA™ has helped to develop or commercialise every single one. This is an outstanding opportunity to join Quintiles and become an integral part of our team.
 
We are looking for suitable individuals to fill the position of :
 
Sr Clinical Data Coordinator
  RESPONSIBILITIES

• Serve as Data Operations Coordinator (DOC) for one or two global studies with fewer than 10 operations staff (excludes
DE), or serve in a leadership role to a specific DM Task.
• Manage delivery of projects through full data management study life-cycle (with minimal guidance).
• With guidance from DTL or Manager, manage project timelines and quality; determine resource needs; identify out-ofscope
work.
• Serve as back-up for Data Operations Coordinator or Data Team Lead (with guidance).
• Perform comprehensive data management tasks including data review, writing and resolving data clarifications.
• Perform database designer activities for technologies not requiring extensive programming.
• Perform comprehensive quality control procedures.
• Independently bring project solutions to the CDM team.
• Solve issues through using the global issue escalation/communication plan.
• Consult with Standards Group for process issues; communicate ideas for process improvement.
• Assist in developing and implementing new technology.
• Understand and comply with core operating procedures and working instructions.
• Meet objectives as assigned.
• Develop and maintain good communications and working relationships with CDM team.
• Interact with CDM team members to negotiate timelines and responsibilities.
 

Job Requirements

• Good understanding of clinical drug development process
• Background in Medical Terminology, Pharmacology, Anatomy, and Physiology
• Excellent organizational, communication, and data management skills (detail oriented)
• Ability to establish and maintain effective working relationships with coworkers, managers and clients
 
MINIMUM REQUIRED EDUCATION AND EXPERIENCE
• Bachelor's degree, or educational equivalence, in clinical, biological, or mathematical sciences or related field or nursing
qualification with 1 year clinical

We know that meaningful results require not only the right approach but also the right people. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve human health outcomes.

Whatever your career goals, we are here to ensure you get there!

We invite you to join IQVIA™.

Job ID: 1603363

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