• Company: IQVIA
  • Location: United States
  • Posted: December 14, 2017
  • Reference ID: 1723353
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.


This is a role that really sets the pace for each and every study. The goal is always to help bring new drugs to market, faster and more efficiently - making a real difference to the lives of patients. It is a role where self-motivation, a dynamic personality and the ability to work with, and lead a wide variety of highly-skilled professionals can let you develop the career you choose.

Award-winning and innovative, our projects have the size and reach to help you grow professionally. The role also offers a greater level of flexibility than many, with home-based or office working as options. There is also flexibility around working hours, as many projects require work across different international time zones. Yet at the same time, even if you are home-based, we make every effort to ensure a supportive team environment.

While projects vary, your typical responsibilities might include:

  • Directing and managing the delivery of all required start-up, maintenance and regulatory activities for selected studies as determined by either the agreed algorithm or the Sponsor's (customer's) requirements
  • This includes pre-award activities, oversight of the scope of work, budget and resources
  • Developing and implementing the RSU Management Plan
  • Ensuring collaboration across RSU, including communication with regions and countries
  • Assisting with the creation and review of core scientific, technical and administrative documentation
  • Contributing to the collection, interpretation, analysis and dissemination of accurate regulatory intelligence
  • Ensuring overall project efficiency and adherence to project timelines and financial goals

    You will need to be comfortable negotiating, collaborating and communicating with a variety of colleagues and customers - including project and clinical leads. Ideally, you will also have an understanding of clinical research, project management and drug development. Good time management and attention to detail are also essential skills.

Job Requirements
You should have:
  • A Bachelor's degree or equivalent in a life sciences, biopharma, nursing or related discipline
  • A minimum of three years' (ideally five) relevant experience
  • Alternatively, you should have an equivalent combination of education, training and experience
If you want to make an impact in the global research market, where we are working to make a real difference in patient health, we ask you to .

Connect to great opportunity™

Quintiles is a strong advocate of diversity and inclusion in the workplace. We believe that a work environment that embraces diversity will give us a competitive advantage in the global marketplace and enhance our success. We believe that an inclusive and respectful workplace culture fosters a sense of belonging among our employees, builds a stronger team, and allows individual employees the opportunity to maximize their personal potential.

EEO Minorities/Females/Protected Veterans/Disabled

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™.

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