Principal or Senior Statistical Programmer - Remote

Veramed; Spain (TX); Hybrid; USD 110,000 - 170,000; Full time

Job summary

Veramed is seeking Principal and Senior Statistical Programmers to join a specialist CRO. Roles are permanent with options for fully remote, hybrid or office-based working.

The Senior/Principal Programmer will provide programming support to the statistics and programming department across diverse projects and may supervise line or project activities. Key responsibilities include SAS and R programming, protocol/SAP/CSR review, CDISC validation, and maintaining audit-ready study master files.

Qualifications

• BSc, MSc or PhD in numerical discipline (or relevant equivalent industry experience).
• At least 6 years of relevant industry experience.
• Experience with SAS and R in clinical trials.
• Knowledge of CDISC standards and validation processes.

Responsibilities

• Lead internal and client study, project and cross-functional team meetings.
• Present study updates internally and at client meetings.
• Author, review and validate SAS programs for datasets, TFLs and macros.
• Maintain study master files and audit-ready documents.
• Provide internal technical training where appropriate.

Skills

SAS

R

Leadership

Project mgmt

Education

BSc, MSc or PhD in numerical discipline

Tools

CDISC Standards

Job description

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 members
• Ensure learnings are shared across projects or studies
• Develop and provide internal technical training where appropriate
• 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.