Are you interested in making a world of difference in cancer care?

Cancer strikes more than 10 million people worldwide each year. As the leading medical society representing doctors who care for people with cancer, the American Society of Clinical Oncology (ASCO) is committed to conquering cancer through research, education, and promotion of the highest quality, equitable patient care.

Who we are:

ASCO is a flexible, high-performance membership organization where employees collaborate to support our mission through evidence, care, and impact. Together with Conquer Cancer, the ASCO Foundation and CancerLinQ colleagues, we foster a culture that prioritizes customer-centricity, emphasizes teamwork, commits to quality, and values inclusion. Our culture, ASCO Works – Our Way of Working, has long enabled workplace flexibility and embraced technology to help us achieve balance.

ASCO offers competitive salaries, an excellent benefits package, and opportunities to participate in professional development programs. To learn what it’s like to work at ASCO, click here.

This position is remote eligible or primary location in Alexandria, VA.

What you will do:

• Supports end-to-end data management related activities (database design, data collection, data analysis, opening and resolving queries, reviewing datasets, reporting)
• Responsible for identifying, resolving, and tracking data discrepancies both within the electronic data capture (EDC) system or outside of it, which may include data entry 
• Participates in implementation of electronic case report form (eCRF) revisions through User Acceptance Testing (UAT) and forms working group meetings
• Collaborates with Clinical Research Data Manager, SAS Programmer, Biostatistician for programming and reporting needs for both internal and external stakeholders, including the Data and Safety Monitoring Board (DSMB)
• Maintains working knowledge of protocol, manuals, data collection forms, and other study documents, as well as study databases, maintaining data dictionaries, etc.
• Adhere to SOPs and provide minor revisions as needed for data management, monitoring, and reporting activities
• Supports routine and ad hoc TAPUR Study Data Team related work as needed

What you will need to be successful: 

• Bachelor's degree, preferably in healthcare or related field or equivalent level of experience, training, and education
• At least 3-5 years of experience working in clinical research
• Proficiency with cleaning and working with clinical trial data
• Familiarity with EDC systems
• Strong organizational, investigative, documentation, and summarization skills
• Strong interpersonal and customer service skills
• Excellent communication skills with the ability to clearly and effectively convey and receive information
• Ability to work on multiple projects with competing deadlines
• Commitment to work within a team to meet timelines and deliverables
• Excellent analytical skills with ability to collect and analyze information and problem-solve
   

Ideal Candidate will also contribute: 

• Experience working with healthcare professionals is a plus
• Experience with project management or in the oncology field

ADA/Physical Requirements 

Fast-paced office environment with extended periods seated or standing at a desk.  

High use of computer and other office technology equipment. 

Travel

Approximately once a quarter to ASCO headquarters, with the potential opportunity for additional educational or development opportunities.

At ASCO, our goal is to foster and encourage a diversity of thought, experience, and background in our workplace. Our organization’s culture is multi-dimensional, and we encourage our employees to leverage their unique perspectives and ideas. ASCO is proud to be an Equal Opportunity Employer (EOE).