Clinical Data Manager

Role Details

12 Month Contract (Extension possibility)

Full time 1FTE - 40 hours per week

Fully Remote in Romania, Bulgaria, Hungary or Slovakia

About the Opportunity

A leading global CRO are seeking multiple Clinical Data Managers to support their expanding portfolio of clinical studies across multiple therapeutic areas. This is a hands‑on data management role where you’ll manage end‑to‑end study activities, ensure high‑quality data delivery, and collaborate closely with cross‑functional teams and sponsors.

You’ll work with experienced project managers, clinical teams, statisticians, and external vendors to ensure databases are built correctly, cleaned efficiently, and locked on time. The organisation is growing rapidly, offering strong development opportunities, stability, and exposure to complex global studies.

This role suits someone who enjoys autonomy, problem‑solving, and working in a fast‑paced, collaborative environment.

What You’ll Be Doing

• Managing full data management activities from study start‑up through database lock
• Designing and reviewing CRFs, edit check specifications, and data validation rules
• Building and testing EDC databases (e.g., Rave, Inform, DataLabs)
• Authoring and maintaining study documentation, including DMPs, DVPs, Completion Guidelines, and UAT plans
• Performing data cleaning, query management, discrepancy resolution, and reconciliation of third‑party/vendor data
• Executing UAT and ensuring database functionality aligns with protocol requirements
• Supporting data transfers, listings review, and lock activities
• Collaborating with sponsors and cross‑functional teams to resolve issues and maintain timelines
• Maintaining an inspection‑ready TMF throughout the study lifecycle
• Contributing to process improvements and supporting junior team members where needed

Required Skills & Experience

• Bachelor’s degree in a technical, clinical, or health‑related field
• 3+ years’ practical experience in Clinical Data Management or Data Coordination
• Hands‑on experience with commercial EDC systems (Medidata Rave, Oracle Inform/RDC, DataLabs, or similar)
• Strong understanding of GCP, ICH, protocol design, and clinical data flows
• Excellent English communication skills
• Proficiency with Microsoft Office (Excel, Word, Outlook)
• Strong analytical skills, attention to detail, and ability to work independently
• Comfortable working in a fast‑paced, deadline‑driven environment
• Proven ability to deliver high‑quality outputs and maintain strong sponsor relationships

Why This Role

You’ll join a global CRO with long‑term growth, a strong study pipeline, and a commitment to operational excellence. This is an opportunity to work on impactful clinical studies, develop your technical expertise, and contribute directly to high‑quality data delivery that supports regulatory submissions and patient outcomes.

With remote flexibility, international exposure, and clear progression pathways, this role is ideal for someone seeking stability, meaningful work, and a chance to grow within a supportive, collaborative team.

Planet Pharma

We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.