Associate Data Manager (Medtech)

TL;DR

Associate Data Manager (Medtech): Managing clinical trial data integrity and database quality for biotech and pharma clients with an accent on protocol compliance and data management plan execution. Focus on resolving data discrepancies, performing user acceptance testing for CRFs, and ensuring high-quality deliverables within clinical data management systems.

Location: Must be based in Bulgaria (Remote)

Company

A global clinical research organization supporting biotech, medtech, and specialty pharma companies in bringing breakthrough medical innovations to market.

What you will do

• Review clinical trial data in CDMS to ensure adherence to protocols and data management plans.
• Generate and resolve queries with investigational sites, vendors, and clinical research associates.
• Support the development and user acceptance testing of CRFs and edit check specifications.
• Maintain documentation for CRF testing and data listing validation.
• Provide input on data management plans to support clinical study deliverables.

Requirements

• Must be based in Bulgaria.
• Bachelor degree in a technical, clinical, or health-related field or equivalent experience.
• 3 to 5 years of practical experience with commercial clinical data management systems or EDC products.
• English: B2+ proficiency required.
• Strong analytical and organizational skills with the ability to manage multiple projects.
• Proficiency in Microsoft Office Suite.

Culture & Benefits

• Remote work arrangement.
• Fixed-term contract until the end of October 2026.
• Standard working hours: 11 AM to 7 PM, Monday–Friday.
• Opportunity to work on life-changing medical innovations.
• Supportive environment focused on professional growth and work-life balance.