Senior/ Clinical Research Associate (Shanghai/Guangzhou/Chengdu) - (1613198) in Shanghai, CN at IQVIA™

Date Posted: 5/11/2018

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.
At IQVIA™ we help healthcare and biopharma companies improve their probability of success. We do this by connecting our scientific, therapeutic and analytics expertise with superior delivery. From advisory through operations, IQVIA™ and its affiliate companies is now the world’s largest provider of product development and integrated healthcare services.
 
One of FORTUNE’s ‘Most Admired Companies’, we offer unparalleled scope for a career in world-leading clinical research. Global projects, innovative tools and industry leading customers combine with outstanding support and clear career management which allows you to make a difference and to connect with great opportunities.
 
Clinical Research Associate – the role
 
Whether you’re beginning or continuing your career as a CRA, this role is an ideal stepping-stone. You’ll have training and development to plan and progress your career in the direction you choose. And you won’t do it alone – you’ll have dedicated mentoring and structured quarterly reviews on performance, promotion and bonus awards.
 
Award winning and innovative, we’ll give you access to cutting-edge in-house technology, allowing you to work on global projects but with a regional / home state travel remit, so no need for national travel. You’ll be building a smart and flexible career with no limits.
 
While projects vary, your typical responsibilities might include:
 
  • Site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation
  • Supporting the development of a subject recruitment plan
  • Establishing regular lines of communication plus administering protocol and related study training to assigned sites
  • Evaluating the quality and integrity of site practices – escalating quality issues as appropriate
  • Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution


Job Requirements

You will need to be comfortable collaborating and communicating with a variety of colleagues and customers. Ideally you will also have a good basic knowledge of applicable clinical research regulatory requirements.
 
Minimum requirements:
 
You should have:
  • A Bachelor's degree or equivalent in a health care or other scientific discipline
  • Successful completion of a CRA Trainee Program or at least three months of on-site monitoring experience
  • Alternatively, you should have an equivalent combination of education, training and experience solving skills
  • Strong written and verbal communication skills
  • Ability to travel when required

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: 1613198