Clinical Research Coordinator

Job Type

Full Time

Published

05/30/2018

Address

2318 Mill Road
Suite 800
Alexandria
VA
22314
United States

Description

Are you interested in pursuing a rewarding career within a premier and growing non-profit organization, while applying your research and science background? Do you desire a position that entails multiple responsibilities while exposing you to a pragmatic clinical trial?


Who we are:


ASCO is a stable, forward-thinking, growing membership organization that operates in a results-focused work environment in which employees’ evaluation emphasizes performance outcomes over presence or time. This is an Alexandria, Virginia-based position that offers an excellent benefits package, subsidized parking or Metro benefits, and opportunities to participate in professional development programs. To learn more about ASCO, visit www.asco.org/jobs.


Who we are looking for:


We are looking for a high performing Clinical Research Coordinator with at least 2-3 years of related work experience including a focus on research to join the Research and Analysis Division (RAD) of the Center for Research and Analytics. The selected candidate will provide comprehensive, high-quality program coordination and research support for a multi-site clinical trial in cancer research, the Targeted Agent and Profiling Utilization Registry (TAPUR) Study (www.tapur.org).


What you will do:


  • Provide support in the operations and monitoring services for the TAPUR Study including supporting evaluation and selection of clinical sites, coordinating initiation and training for participating clinical sites, and supporting management of study related work and preparation of reports, summaries, presentations
  • Act as a primary contact for TAPUR Study sites by investigating site issues and responding to inquiries in a timely fashion exercising analysis and judgment
  • Coordinate communications with study sites for data query review and resolution
  • Support development and documentation of workflows for study procedures and processes
  • Coordinate activities for the study website, including managing content and messaging, and updating study materials
  • Lead 2-3 major TAPUR Study Groups or projects
  • Provide general administrative and other support for the study and projects, as needed


What you will need in order to be successful:


  • A college degree in a health or a science related field
  • Proficiency with Microsoft Office applications; and an openness to embracing new technology
  • Superior communication skills; including oral, written, and listening
  • Strong attention to detail, analytical with the ability to see the big picture and exercise judgment, and focused on quality control
  • Ability to manage own time, priorities, and resources to achieve goals
  • Commitment to work within a team to meet timelines and deliverables with a strong focus on customer service


Ideal candidates will also contribute:


  • Experience working with clinical trials in a supportive role
  • Basic familiarity with medical terminology (oncology knowledge is a plus)
  • Experience working with electronic data capture systems


 ASCO is proud to be an Equal Opportunity Employer (EOE)

Professional Level

None specified

Minimum Education Required

4-year degree


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