In 2016, ASCO launched the Targeted Agent and Profiling Utilization Registry (TAPUR) Study – ASCO’s first clinical trial. The ongoing study collects “real-world” data on clinical outcomes to help learn additional uses of molecularly-targeted cancer drugs outside of indications approved by the Food and Drug Administration (FDA). Since launch, the study has steadily grown to include clinical sites in over 100 locations, with more than 1,700 participants registered and over 1,200 participants enrolled.
Who we are:
ASCO is a stable, forward-thinking, 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 Administrator with at least 5 years of related clinical trial experience 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 operational 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, collaborating with internal and external stakeholders, as needed
Act as a primary contact for TAPUR Study sites by investigating site issues and responding to inquiries and issues in a timely fashion, exercising analysis and judgment
Lead review and resolution of data queries for assigned clinical sites, including weekly and other routine review and coordination of communication, data change requests, and participate in query and data management report generation and validation
Support development and documentation of workflows for study procedures and processes
Lead coordination of 2-3 TAPUR Study Groups, Committees, or projects and related work
Provide general administrative and other support for the study and its projects, as needed
What you will need in order to be successful:
A college degree, in a health or a science related field is preferred
Proficiency with Microsoft Office applications; and an openness to embracing new technology
Experience with individual clinical site management
Protocol understanding and application
Basic project management and administration experience
Analytical skills for data query review and response, and electronic data capture skills to navigate the system and support sites
Superior communication skills; including oral, written, and listening
Strong attention to detail, 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:
Basic familiarity with medical terminology (oncology knowledge is a plus)
ASCO is proud to be an Equal Opportunity Employer (EOE)
About American Society of Clinical Oncology
ASCO is a stable, forward-thinking, membership organization that operates in a results-focused work environment in which employees’ evaluation emphasizes performance outcomes over presence or time.
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