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, 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 its like to work at ASCO, click here.

　　Who we are looking for:

　　We are seeking a dedicated Clinical Research Data Administrator I to provide support for the CDK4/6 Inhibitor Dosing Knowledge (CDK) Study and other clinical research initiatives. In this role, you will play a crucial part in data management activities and collaborate with cross-functional teams to ensure the success of our projects.

　　If you are a results driven, motivated individual with a passion for data management and you're looking for a rewarding career in clinical research, apply now!

　　This position is funded through collaborators that have committed to support the study. Continuation of this position therefore is contingent upon funding being available.

　　Remote candidates welcome or primary location in Alexandria, VA

　　Responsibilities

　　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 in tracking documentation prior to data freeze deadlinesMaintains working knowledge of protocol, manuals, data collection forms, and other study related documentationAssists with the development and maintenance of data dictionaries, code tables, and study databasesAdhere to SOPs and provide minor revisions as needed for data management, monitoring, and reporting activitiesParticipates in the development and implementation of electronic case report forms (eCRFs)Participates in User Acceptance Testing (UAT), assists with the development of UAT plans, and reviews UAT findingsCollaborates with Clinical Research Data Manager, SAS Programmer, and Biostatistician for programming and reporting needs for both internal and external stakeholders, including the Data and Safety Monitoring Board (DSMB)Supports routine and ad hoc CDK Study Data Team related work as neededRequired Education and Experience

　　Bachelor's degree, preferably in healthcare or related field or equivalent level of experience, training, and educationAt least 3-5 years of experience working in clinical researchProficiency with cleaning and working with clinical trial dataFamiliarity with EDC systems including but not limited to REDCapPreferred Education and Experience

　　Experience working with healthcare professionalsExperience with project management or in the oncology fieldCompetencies

　　Strong organizational, investigative, documentation and summarization skillsStrong interpersonal and customer service skillsExcellent communication skills with the ability to clearly and effectively convey and receive informationAbility to work on multiple projects with competing deadlinesCommitment to work within a team to mee timelines and deliverablesExcellent analytical skills with ability to collect and analyze information and problem-solveADA

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

　　High use of computer and other office technology equipment.

　　Travel requirements

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

　　Remote eligible

　　Yes

　　Generous Benefits Package:

　　Hybrid Work EnvironmentOpen Leave PolicyPaid Family Leave13 Paid Holidays per Calendar YearStaff Appreciation Days401(k): 7.5% Employer ContributionMedical/Dental/VisionEmployee Assistance ProgramFertility and Family FormingHealthcare ConciergeFlexible Spending Account(s)Healthcare Savings AccountDisability and Life InsuranceThe American Society of Clinical Oncology (ASCO) is an Equal Employment Opportunity (EEO) employer. It is the policy of the Company to provide equal employment opportunities to all qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran or disabled status, or genetic information.

　　At ASCO, our goal is to foster and encourage a diversity of thought, experience, and background in our workplace. Our organizations culture is multi-dimensional, and we encourage our employees to leverage their unique perspectives and ideas.