Creates EDC system structure, workflow, edit checks, and user roles based on data standards and study protocols.
Creates study-level documentation such as specifications, test plans, and training materials.
Performs post-live changes to EDC system under change control processes.

Qualifications:

Graduate or bachelor's degree in Life Sciences, Pharma, or related health discipline.
Prior experience in EDC system creation and Edit Check programming (Zelta, Medidata) is a must.
Effective communication skills and cooperative team-oriented approach.

Additional Information:

When you join Ergomed Group, you make a difference by helping bring safe pharmaceutical treatments to patients worldwide.
You'll join a passionate and collaborative team of experts in clinical research, pharmacovigilance, and quality consulting.
Our values include quality, integrity, drive, agility, belonging, and collaborative partnerships.

Ergomed Group

Ergomed Group helps biopharmaceutical companies develop, deliver, and safeguard therapies in oncology, rare disease, and other complex areas through clinical research, pharmacovigilance, and quality consulting. They are a diverse global team united by values of quality, integrity, drive, agility, and belonging, with a shared sense of purpose to bring safer treatments to patients.

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