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Overview:

  • Provides validation and UAT support for Clinical Data Management activities across studies.
  • Leads and coordinates functions for multiple assigned projects related to the planning, execution, collection, and cleaning of clinical data.
  • Works within the company’s SOPs, guidelines and standards to ensure data integrity at all times.

Responsibilities:

  • Audit potential data management vendors, as appropriate.
  • Assist in the compilation of clinical data for regulatory submissions.
  • Develop and execute data validation plans to identify and address data inconsistencies, errors, or outliers.

Required Skills & Knowledge:

  • Strong working knowledge of clinical data management systems (CDMS) and data validation tools.
  • Excellent verbal and written communication skills and strong interpersonal skills are required.
  • Experience with Electronic Data Capture (EDC) & other data management systems.

Iovance Biotherapeutics

Iovance Biotherapeutics is committed to cultivating and offering a diverse and inclusive work environment. As an equal-opportunity employer, their employees and applicants will be considered without regard to an individual’s race, color, religion, sex, pregnancy, national origin, age, physical and mental disability, marital status, sexual orientation, gender identity, gender expression, genetic information, military and veteran status, and any other characteristic protected by applicable law.

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