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Project Specialist (Medidata Rave) - South Africa (Remote) - FSP

Project Specialist (Medidata Rave) - South Africa (Remote) - FSP

PAREXELZA
20 days ago
Job type
  • Remote
Job description

Job title : Project Specialist (Medidata Rave) - South Africa (Remote) - FSP

Job Location : South Africa,

Deadline : October 09, 2025

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About This Role

  • Parexel is currently seeking a Project Specialist (Medidata Rave) to join us in South Africa, dedicated to a single sponsor.
  • This role will be responsible for the administration and support of the Medidata cloud platform. It involves creating and managing user accounts, sites, ensuring proper access controls, and maintaining data integrity within the Medidata Rave EDC system. You will work closely with various teams to facilitate user access, compliance with training requirements, and the efficient management of user data. Additionally, you will support system validation processes to ensure that the Medidata platform operates in accordance with regulatory and compliance standards.
  • Working as a Project Specialist (Medidata Rave) at Parexel FSP offers tremendous long-term job security and prospects. We undertake vital clinical studies for sponsors including the leading global biotechs and Pharma top 50. And we have an incredible pipeline of work.
  • Expect exciting professional challenges in inspiring studies, but with time for your outside life.
  • This will be a fully remote home-based position.
  • Responsibilities

  • Create new user accounts within Medidata Rave EDC and other EDC systems such as Veeva CDMS systems.
  • Ensure correct user roles and permissions are assigned based on study requirements.
  • Collaborate with study teams to ensure accurate and timely user assignments.
  • Periodic review of user access across the platform to ensure only valid users always have access to the studies.
  • Administer and manage study and site assignments.
  • Assign required eLearnings and report matrices to all studies in adherence to the internal procedures. Participate in system validation activities to ensure the Medidata platform meets regulatory and compliance standards.
  • Here are a few requirements specific to this advertised role.

  • Bachelor’s Degree in a relevant field and a minimum of 2 years’ relevant experience (3 is preferred). An equivalent combination of education and experience may be considered.
  • 3+ years of Medidata Rave EDC / Veeva CDMS experience in study administration, site administration, and user administration.
  • Attention to detail and the ability to work individually, within a multi-disciplinary team.
  • Strong English language written and verbal communication skills.
  • Possesses solid computer system and technical skills with a strong ability to learn multiple computer applications.
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    Project South Africa • ZA

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