MedFocus Asst. PM / Data Assoc. III in Massachusetts

Clinical Research Data Associate

The Data Associate is responsible for the quality control of patient data on one or more studies, working with Clinical Research Associates at member institutions, physicians and statisticians throughout this process. Duties include:

  • Review and evaluation of clinical patient data utilizing the electronic data capture system Medidata RaveĀ®.

  • Assist with the creation and validation of electronic case report forms and edit checks for their assigned studies.

  • Using a study specific Data Management Plan, review site reported data elements, generate manual queries, resolve answered queries.

  • Perform serious adverse event reconciliation between RaveĀ® and the National Cancer Institute's safety database.

  • Review treatment information, evaluate response to treatment, and ensure follow-up and survival data are accurately coded and updated in the database in a timely way.

  • Work with the Study Chair to perform final case review. Review and provide input for protocols in development.

  • Assist the study chair and statistician with the preparation of the database for analysis.

  • Other duties as assigned.


  • Bachelor's degree or equivalent work and/or life experience

  • Excellent organizational and interpersonal skills

  • Proficiency in database and word processing skills, and MS Office

  • Excellent written and verbal communication skills

  • Strong customer service skills and an ability to interact cordially with others

  • Attention to detail

  • Reliability

  • Knowledge/experience with electronic data submission a plus, but will fully train qualified candidates.

  • Medical or biological sciences background is helpful but not required.

Please send resume to

Min Salary: $0.00

Max Salary: $0.00

State: MA