Senior / Principal Clinical Database Manager

Precision For Medicine; Albacete; A distancia; EUR 50.000 - 80.000; Jornada completa

Descripción de la vacante

A leading company in precision medicine is seeking a Senior / Principal Clinical Database Manager to join their innovative team. You will be responsible for the design and management of clinical databases, ensuring quality in data collection and analysis. This remote position allows flexibility while contributing to groundbreaking work in oncology and clinical trials.

Formación

• Experience in developing clinical data management databases.
• Proficiency in Microsoft Office for documentation.
• Knowledge of clinical research and data management practices.

Responsabilidades

• Design, develop, and maintain clinical databases.
• Interface with internal teams and vendors for requirements.
• Provide operational training to users and junior staff.

Conocimientos

Leadership

Communication

Organization

Clinical data management

Understanding of CDISC standards

Educación

Bachelor’s degree or related experience

Medidata Rave EDC Certified Study Builder

Herramientas

Microsoft Office

Base SAS

SAS / STAT

SAS / ACCESS

Descripción del empleo

Senior / Principal Clinical Database Manager

Remote, Spain

Precision for Medicine are hiring a Senior / Principal Clinical Database Manager to join our team, candidates can work remotely in the following locations : UK, Spain, Hungary, Poland, Romania, Serbia or Slovakia.

Position Summary :

The Senior / Principal Clinical Database Manager is responsible for the design, development, testing, implementation, maintenance and support of clinical databases and applications. Position will interface directly with the internal team (i.e. Data Management, Project Management, etc.), EDC vendor, clients and third-party vendors to gather requirements and provide status updates. Provides operational and technical training to end users and junior staff. Additionally, the Senior / Principal Clinical Database Manager may play a lead role in internal software projects that require specialized programming and / or scripting.

Qualifications :

• Must have experience in developing and customizing clinical data management databases in a clinical, scientific or health care discipline
• Bachelor’s and / or a combination of related experience
• Medidata Rave EDC Certified Study Builder
• Rave Advanced Custom Function programming experience

Other Required :

• Proficiency in Microsoft Office : Word, Excel, PowerPoint, Outlook.
• Able to handle a variety of clinical research tasks.
• Excellent organizational and communication skills
• Professional use of the English language; both written and oral.
• Understanding of CDISC standards (CDASH, SDTM, ADaM, etc.)
• Experience in clinical database management system development.
• Experience in a clinical, scientific or healthcare discipline.
• Experience in utilizing various clinical database management systems
• Broad knowledge of drug, device and / or biologic development and effective data management practices
• Strong leadership and interpersonal skills
• Must be able to communicate effectively in the English language.

Preferred :

• Oncology and / or Orphan Drug therapeutic experience
• Base SAS, SAS / STAT and SAS / ACCESS software
• Advanced experience in Database Management, object-oriented programming
• Veeva set up experience

Precision medicine is revolutionizing the attack on cancer—and we are passionate about helping you harness its power. We strike tumours on a molecular level using biomarkers to link specific mutations to specific treatments. We combine deep science with deep data from advanced technological platforms, then layer on specialized expertise in the design and execution of targeted, adaptive clinical trials. Ultimately, we deliver robust insights that inform real-time decisions—and optimize the oncology development pathway.

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