¡Activa las notificaciones laborales por email!

Senior / Principal Clinical Database Manager

Precision Medicine Group

Tarragona

A distancia

EUR 75.000 - 95.000

Jornada completa

Hoy
Sé de los primeros/as/es en solicitar esta vacante

Descripción de la vacante

A leading biotechnology firm is seeking a Senior / Principal Clinical Database Manager. This role includes responsibilities for design and maintenance of clinical databases and working with various stakeholders. A Bachelor’s degree and experience in clinical data management are essential. The position supports remote work and requires expertise in programming and data management practices.

Formación

  • Must have experience in developing and customizing clinical data management databases.
  • Professional use of the English language required.
  • Understanding of CDISC standards (CDASH, SDTM, ADaM).
  • Experience in clinical database management system development.

Responsabilidades

  • Design, develop, test, implement, and maintain clinical databases.
  • Interface with internal teams and vendors to gather requirements.
  • Provide operational and technical training to end users.
  • Play a lead role in internal software projects.

Conocimientos

Experience in developing clinical data management databases
Proficiency in Microsoft Office
Excellent organizational and communication skills
Experience in Object Oriented Programming (C#, C++, VBS)

Educación

Bachelor’s degree or related experience

Herramientas

SAS
R
SQL
Descripción del empleo
Position Summary

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.

The Senior / Principal Clinical Database Manager is responsible for the design, development, testing, implementation, maintenance and support of clinical databases and applications. The 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. This role provides operational and technical training to end users and junior staff, and may play a lead role in internal software projects that require specialized programming and/or scripting.

Qualifications
Minimum Required
  • 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.
  • Rave API integration experience using external vendor modules.
  • 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.
  • Experience in Object Oriented Programming (C#, C++, VBS, etc.), scripting language (PERL, etc.), SAS, R, SQL.
  • 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.
  • SAS Macro programming language.
  • Advanced experience in Database Management, object-oriented programming.
  • Veeva set up experience.
  • Medidata Rave certification.

Precision medicine is revolutionizing the attack on cancer—and we are passionate about helping you harness its power. We strike tumours at 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.

Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice.

Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.

If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at QuestionForHR@precisionmedicinegrp.com.

It has come to our attention that some individuals or organizations are reaching out to job seekers and posing as potential employers presenting enticing employment offers. We want to emphasize that these offers are not associated with our company and may be fraudulent in nature. Please note that our organization will not extend a job offer without prior communication with our recruiting team, hiring managers and a formal interview process.

Consigue la evaluación confidencial y gratuita de tu currículum.
o arrastra un archivo en formato PDF, DOC, DOCX, ODT o PAGES de hasta 5 MB.