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

Inscríbase (haciendo clic en el botón correspondiente) después de revisar toda la información relacionada con el trabajo a continuación.

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 escalate 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 members

- Ensure 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. xhfqzwm

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

📌 Principal Or Senior Statistical Programmer - Remote (Foz)
🏢 Veramed
📍 Foz