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Clinical Data Careers

Vita Global Sciences provides unparalleled professional services in clinical data analytics and functional outsourcing. As an innovator in the Life Sciences space, Vita Global Sciences partners with clients to develop and deliver full service, scalable data solutions in the Pharmaceutical, Biotechnology, Medical Device, & CRO industries. Our growth and success is based largely upon our multi-cultural, and diverse workforce. Our team is our most valuable asset and we allow our team members to grow professionally, as we rapidly grow as a company. We are dedicated to hiring remarkably talented people who are self-directed, determined and smart, often favoring ability over experience. Our work environment provides opportunities to enhance their roles with clear responsibilities and the opportunity to work on a variety of assignments.

At VGS, you will have an inspiring trust-based work culture for learning with motivational, approachable and visionary leadership. Working at VGS you will see the impression of an exciting environment to work and grow.

Manage all aspects of the clinical data management process from study start-up to database lock for in-house Electronic Data Capture (EDC) trials including data management performance, metrics, quality assurance checks and communication of trial status within and outside the trial team.

  • Manage / assign responsibilities for Data Managers and also serve as a member of Study Teams. Act as primary Data Management contact and contributor for projects
  • Create / monitor timelines and ensures that all deadlines are met with quality
  • Participate in the review of clinical data, analysis tables, listings, figures, and patient profiles for data consistency and accuracy
  • Identify and troubleshoot operational problems and barriers for studies based on metrics data, audit reports, and input from project team members and other stakeholders
  • Participates in the development and maintenance of Standard Operating Procedures (SOPs) and Work Instructions related to data management activities
  • Develop and support creation of data management documentation, specifications and UAT requirements for database and test according to UAT Plan
  • Create, review and revise data management documentation
  • Ensures data management activities are conducted in accordance with GCP, GCMP, internal SOPs, and meet all regulatory requirements
  • Requirements:
  • Identify project challenges and risks, and proposing appropriate and strategic solutions to issues
  • Electronic data capture experience (Medidata Rave®) and working knowledge of Oncology indications
  • Proficient in data management activities including CRF and clinical database design, clinical data cleaning and analysis for Oncology trials