Senior Clinical Data Manager II

Precision Medicine Group

Clinical Data Manager II responsible for the data management process of clinical trials. Overseeing project data entry, ensuring quality and compliance with regulatory standards.

Posted 6/4/2026full-timeRemote • 🇭🇺 HungarySeniorWebsite

About the role

Key responsibilities & impact

Responsible and manages all aspects of the clinical trial data management process from study start-up to post database lock for assigned projects.
Primary Data Management (DM) contact (Lead DM role) for assigned clinical project(s) / program(s), ensuring that there is back-up, continuity, responsiveness, and that tasks are performed in a timely manner.
Oversee project data entry process including development of data entry guidelines, training, data entry quality and resourcing.
May perform quality control of data entry.
Provide input, assess and manage timelines. Ensure clinical data management deadlines are met with quality.
Conduct database build UAT and maintain quality controlled database build documentation.
Responsible for creating, revising, versioning and maintaining data management documentation. Oversee completeness of data management documentation for the Trial Master File.
Train clinical research personnel on the study specific CRF, EDC, and other project related items as needed.
Review and query clinical trial data according to the Data Management Plan.
Coordinate SAE/AE reconciliation.
Liaise with third-party vendors such as external data and EDC vendors in a project manager capacity in support of timelines and data-related deliverables.
Identify and troubleshoot operational problems, issues, obstacles, and barriers for studies based on metrics data, audit reports, and input from project team members.

Requirements

What you’ll need

Bachelors and/or a combination of related experience
8+ years’ experience as a Sr. Clinical Data Manager or 5+ Years as a Clinical Data Manager II working for a Clinical Research Organisation, Pharmaceutical or Biotech company
Set up and Database migrations experience
Oncology experience preferred
Proficiency in Microsoft Office: Word, Excel, PowerPoint, Outlook
Excellent organizational and communication skills
Professional use of the English language; both written and oral
Experience in utilizing various clinical database management systems
Broad knowledge of drug, device and/or biologic development and effective data management practices
Strong representational skills, ability to communicate effectively orally and in writing
Strong leadership and interpersonal skills
Ability to undertake occasional travel.

Benefits

Comp & perks

We can consider candidates based in the UK, Poland, Hungary, Romania, Serbia or Slovakia.
Competitive salary

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

clinical trial data managementdata entry guidelines developmentquality control of data entrydatabase build UATdata management documentationclinical research trainingSAE/AE reconciliationdatabase migrationsclinical database management systemsdata management practices

Soft Skills

organizational skillscommunication skillsleadership skillsinterpersonal skillsproblem-solving skillsresponsivenesstimelinesstraining abilitiesrepresentational skillsability to undertake travel