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IQVIA

Data Acquisition Expert - EDC

IQVIA

Bloemfontein, Free State, South Africa • Penuh Waktu

Jadilah yang pertama mendaftar

Pengalaman
5+ tahun
Gaji
Lowongan
1
Diposting
4 jam yang lalu
Mode kerja
Di kantor
Kelayakan
Professionals with strong EDC build experience in clinical research are eligible. The role does not support UK visa sponsorship.
Melanjutkan
Wajib mendaftar

Tempat Anda akan bekerja

Deskripsi pekerjaan

Role overview

The EDC Data Acquisition Expert is responsible for defining and implementing clinical electronic data capture tools and the related documents and workflows needed to meet clinical trial protocol requirements for data capture.

This position works closely with Data Managers, Study Responsible Physicians (SRP), Study Responsible Scientists (SRS), and Biostatisticians to support accurate and efficient clinical data operations.

Key responsibilities

  • Review protocol-specific EDC data collection needs and prepare the study start-up eCRF package using global eCRF libraries.
  • Build eCRF layouts and configure form behavior and dynamic elements.
  • Develop edit checks and custom functions.
  • Prepare technical specifications for tSDV, Safety Gateway integrations, and Datamart mappings.
  • Set up coding configurations in line with trial-specific coding requirements.
  • Carry out test and production Rave EDC migrations.
  • Lead planning, requirements gathering, and implementation for IWRS integrations with EDC.
  • Act as a specialist for complex EDC database build components, including integrations.
  • Act as a specialist for advanced custom function implementation within EDC database builds.
  • Train junior team members on EDC build, migration processes, and relevant tools.
  • Contribute to continuous improvement initiatives across clinical data management processes, systems, and tools.

Requirements

  • At least 5 years of experience building EDC databases for clinical research.
  • Hands-on technical experience with Medidata Rave, including complex database builds.
  • Strong project management capability.
  • Advanced knowledge of custom function programming.
  • Prior experience supporting clinical trials.
  • Experience collaborating in diverse clinical research teams across cross-functional, global, and multi-regional settings.
  • Working understanding of GCP and ICH guidelines.
  • Knowledge of CDASH.
  • This role is not eligible for UK visa sponsorship.

About the employer

IQVIA is a global provider of clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare sectors. The company focuses on helping accelerate the development and commercialization of innovative medicines and improving patient and population health worldwide.

Hiring integrity notice

The employer follows a zero-tolerance approach to candidate fraud. All details and credentials submitted during recruitment must be accurate and complete. Any false information, misrepresentation, or material omission may lead to disqualification during hiring or termination of employment later, subject to applicable law.

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