Senior / Principal Clinical Database Manager

Precision for Medicine; Málaga; Presencial; EUR 40.000 - 80.000; Jornada completa

Descripción de la vacante

A leading company in precision medicine is seeking a Senior / Principal Clinical Database Manager. This role emphasizes the design, development, and support of clinical databases while providing both technical guidance and support to internal teams. Candidates working remotely in Spain will lead internal projects and require proven experience in clinical data management, particularly within healthcare or scientific disciplines.

Formación

• Experience in developing clinical data management databases.
• Proficiency in English language, written and oral.
• Experience in clinical database management system development.

Responsabilidades

• Design, develop, and maintain clinical databases.
• Interface with internal teams and clients to gather requirements.
• Provide training to junior staff and end users.

Conocimientos

Organizational skills

Communication skills

Leadership

Educación

Bachelor’s in relevant field

Herramientas

Microsoft Office

Medidata Rave EDC

SAS/STAT

Veeva

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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