EDC Developer: Build Safe, Life-Saving Trials

Ergomed; England; On-site; GBP 55,000 - 75,000; Full time

Job summary

Ergomed Group seeks an EDC Developer within the Data Management department to build the EDC application for complex projects under supervision by the Director of Data Management. Responsibilities include system design, documentation, and post-live changes to EDC and related reporting tools.

Qualifications include a life sciences degree, essential Zelta v2.0 experience, and proven EDC/Edit Check programming with Zelta or Medidata, plus strong communication and teamwork abilities.

Qualifications

• Graduate or bachelor’s degree in Life Sciences (or Pharma or related health discipline) from an accredited university or college.
• Zelta v2.0 experience is essential.
• Prior experience in EDC system creation and Edit Check programming (Zelta, Medidata) is a must.
• Effective communication skills.
• Cooperative and team-oriented approach.
• Self-motivation and ability to work independently.
• Proficiency in data standards (CDASH & SDTM) and application to EDC system creation, CDASH Certification preferred.

Responsibilities

• Creates EDC system in terms of structure, workflow, edit checks and user roles & permissions based on data standards (CDASH), study protocol and standard eCRF templates.
• Includes: Randomisation, ePRO, IMP Management, Targeted SDV, and additional EDC functionality.
• Creates all study level documentation related to EDC System (Specifications, Test Plans, study training materials).
• Problem solver for mid-level challenges and sponsor requests.
• Performs post-live changes to EDC system under Change Control process.

Skills

Zelta v2.0 experience

EDC system creation

Edit check programming

Effective communication

Team-oriented

Self-motivated

CDASH/SDTM knowledge

Education

Bachelor's degree in Life Sciences or related

Tools

Zelta

Medidata

Job description

Ergomed Group seeks an EDC Developer within the Data Management department to build the EDC application for complex projects under supervision by the Director of Data Management. Responsibilities include system design, documentation, and post-live changes to EDC and related reporting tools.

Qualifications include a life sciences degree, essential Zelta v2.0 experience, and proven EDC/Edit Check programming with Zelta or Medidata, plus strong communication and teamwork abilities.