Principal Or Senior Statistical Programmer - Remote

Mindmatch; Valencia; Híbrido; EUR 70.000 - 90.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Remote work options

Training & development

Descripción de la vacante

MindMatch en Valencia busca un/a Programador/a Estadístico/a Principal o Senior para proyectos en un entorno CRO, con opción remota, híbrida u oficina.

Se exige experiencia en SAS y algo de R, y al menos 6 años en la industria; se ofrece formación continua, entorno de alta calidad y posibilidad de supervisión de equipos y proyectos.

La función incluye revisión de documentos, validación de programas SAS, y liderazgo de reuniones de equipo, aportando buenas prácticas y desarrollo profesional.

Formación

• Experiencia en SAS y algo de R.
• Gestión y liderazgo de equipos o proyectos.
• Conocimiento de buenas prácticas de programación y revisión de documentos clínicos.

Responsabilidades

• Liderar reuniones de estudio internas y con clientes.
• Presentar actualizaciones del estudio a partes interesadas.
• Compartir conocimientos técnicos dentro del equipo de programación.
• Cumplir con políticas, procesos y formación interna.
• Desarrollar formación interna cuando corresponda y mejorar procesos.
• Liderar iniciativas de mejora de procesos.

Conocimientos

SAS programming

R programming

Leadership

Educación

BSc/MSc/PhD in numerical discipline

Herramientas

SAS

R

CDISC standards

Descripción del empleo

Principal or Senior Statistical Programmer - Remote MindMatch Valencia, comunidad valenciana, Spain

Descripción del trabajo

Ready for your next career move? With continued business growth and a strong pipeline of new projects, Veramed is creating new opportunities for Statistical Programmers to work on innovative studies, expand their skills and advance their careers within a supportive, specialist CRO

We have multiple exciting opportunities for Principal and Senior level Statistical Programmers skilled in SAS and R, to join us on a permanent basis. We can offer fully remote, hybrid or office-based working, training and a very supportive and quality focused environment.

The purpose of the role is to provide programming support to the statistics and programming department across a range of projects, clients and therapeutic areas. The Senior or Principal Programmer may also perform a supervisory role (e.g. line management and/or project management).

Key Responsibilities

Technical

• Previous experience with SAS and some R experience/knowledge.
• Perform review of clinical trial documents including protocols, SAPs, CRFs, CSRs
• Author, review and approve study TFL shells and dataset specifications
• Author, validate and document SAS programs for datasets, TFLs and macros, applying good programming practice
• Identify data issues and outliers
• Complete, review and approve CDISC Validation tool reports
• Identify data and standards issues and resolve or upscale as appropriate
• Awareness of emerging standards and associated impact to ongoing and future planned trials
• Maintain proficiency in SAS and awareness of developments
• Maintain study master file documents and any other documents that are required to be audit ready

General

• Lead internal and client study, project and cross functional team meetings effectively
• Present study updates internally and at client meetings
• Share scientific, technical and practical knowledge within the team and with colleagues
• Perform work in full compliance with applicable internal and client policies, procedures, processes and training
• Build effective collaborative working relationships with internal and client team membersEnsure learnings are shared across projects or studies
• Develop and provide internal technical training where appropriate
• Lead process improvement initiatives

Minimum Qualification Requirements

• BSc, MSc or PhD in numerical discipline (or relevant equivalent industry experience)
• At least 6 years of relevant industry experience

Other Information/ Additional Requirements

• Understanding of clinical drug development process, relevant disease areas, endpoints and study designs

WHAT TO EXPECT:

• A warm, friendly working environment in which to thrive both personally and professionally.
• A supportive, open-door management policy that will aid in your development and provide you with the tools to take your career to the next level.
• A truly unique CRO that’s doing something different when it comes to managing staff, projects and building relationships in the industry.
• The ability to own your role and develop your skills and experience. xkdbapo

Hay opciones de teletrabajo/trabajo desde casa disponibles para este puesto.