Sr. Clinical Project Manager (Oncology) (Greater Boston Area) - (R1047391) in Cambridge, MA at IQVIA™

Date Posted: 11/10/2018

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.

Description

(Home-based role that requires interested candidates to also be within a commutable distance to Boston, MA)

OVERVIEW:

This is an important and high-profile role within IQVIA. Project leaders are the people who lead the delivery of our studies bringing drugs to market faster and ultimately improving patients’ lives. It is a role that requires you to liaise directly between IQVIA functions and the customer, acting as that accountable point for delivery and quality whilst maintaining financial control.
 
As a project leader you will manage cross functional teams across this global organization. You will be supported by domain experts in every function, enabled by best in class technology and data analytics. Key collaborators are the Clinical Lead for site management, the Project Management Analyst for project coordination, tracking and financial analysis, and the Site Activation Manager an expert in start-up. IQVIA’s size and global footprint will present you with the breadth of opportunities necessary to develop your career.
 
While projects vary, your typical responsibilities might include:
  • Serving as the primary project contact with the client
  • Leading and managing cross-functional project teams
  • Project status reporting and surveillance for risk
  • Monitoring team performance against contract and client expectations and according to key performance metrics
  • Leading problem solving including management of risk and issue resolution
  • Developing or reviewing study management plans
  • Managing team resource assignments and accountability
  • Oversight of database management
  • Ensuring compliance with study tools, training materials and standard processes, policies and procedures.
You will need to be comfortable collaborating and communicating with a variety of colleagues and clients. Ideally, you will also have some global experience and a pharmaceutical or CRO background.

Job Requirements

MINIMUM REQUIRED EDUCATION AND EXPERIENCE
  • Bachelor's degree in life sciences or related field and 7 years’ clinical research experience including 4 years’ project management experience and experience in clinical operations; or equivalent combination of education, training and experience.

PHYSICAL REQUIREMENTS
  • Extensive use of keyboard requiring repetitive motion of fingers.
  • Extensive use of telephone and face-to-face communication requiring accurate perception of speech.
  • Regular sitting for extended periods of time.
  • May require occasional travel.


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™.


Job ID: R1047391