Senior / Principal Clinical Database Manager

Precision For Medicine; Sevilla; A distancia; EUR 60.000 - 80.000; Jornada completa

Descripción de la vacante

A healthcare precision medicine company is looking for a Senior / Principal Clinical Database Manager to work remotely within Spain. The role includes designing and managing clinical databases, interfacing with various teams, and providing training. Candidates should have experience in clinical data management and a Bachelor’s degree with relevant experience. Strong organizational and communication skills are essential.

Formación

• Experience in developing and customizing clinical data management databases in a clinical, scientific, or healthcare discipline.
• Bachelor’s degree and/or related experience.
• Medidata Rave EDC Certified Study Builder.

Responsabilidades

• Designing, developing, testing, implementing, maintaining, and supporting clinical databases and applications.
• Interfacing with internal teams, EDC vendors, clients, and third-party vendors to gather requirements and provide status updates.
• Providing operational and technical training to end users and junior staff.

Descripción del empleo

Senior / Principal Clinical Database Manager

Remote, Spain

Precision for Medicine is 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 designing, developing, testing, implementing, maintaining, and supporting clinical databases and applications. The role involves interfacing directly with internal teams (e.g., Data Management, Project Management), EDC vendors, clients, and third-party vendors to gather requirements and provide status updates. The manager will also provide operational and technical training to end users and junior staff. Additionally, the role may involve leading internal software projects requiring specialized programming and scripting.

Qualifications:

• Experience in developing and customizing clinical data management databases in a clinical, scientific, or healthcare discipline.
• Bachelor’s degree and/or related experience.
• Medidata Rave EDC Certified Study Builder.
• Experience with Rave Advanced Custom Function programming.

Other Requirements:

• Proficiency in Microsoft Office: Word, Excel, PowerPoint, Outlook.
• Ability to handle various clinical research tasks.
• Excellent organizational and communication skills.
• Professional proficiency in English, 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 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.

Preferred Qualifications:

• Oncology and/or Orphan Drug therapeutic experience.
• Experience with Base SAS, SAS/STAT, and SAS/ACCESS software.
• Advanced experience in database management and object-oriented programming.
• Veeva setup experience.

We are passionate about harnessing the power of precision medicine to revolutionize cancer treatment. Our approach involves linking specific mutations to treatments using biomarkers, combining deep science with advanced technological platforms, and designing targeted, adaptive clinical trials to deliver real-time insights that optimize oncology development.

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