Overview
We are looking for Senior Statistical Programmers in the UK to join Veramed, where you\'ll deliver high-impact programming solutions in an FSP-style capacity, while advancing your career in a supportive, growth-driven environment.
At Veramed, we focus on two key areas: providing exceptional statistical and programming consultancy, and fostering a workplace where our employees can thrive. We’re committed to helping you achieve your unique career goals through tailored development opportunities.
Key Responsibilities
As a Senior Statistical Programmer at Veramed, you\'ll have varied responsibilities and the opportunity to shape your role. Daily tasks may include:
Programming
* Program and QC datasets and TFLs following specifications and best practices.
* Develop dataset specifications aligned with CDISC data standards.
* Participate in internal and client study team meetings.
* Mentor junior team members to enhance their development.
Daily Interactions
* Communicate with study team members and client contacts.
* Share updates internally and in client meetings.
* Collaborate with the Veramed team to ensure timely, high-quality deliverables.
* Provide mentoring and programming expertise as needed.
Opportunities for Growth
* Lead programmer or technical expert roles.
* Experience across various therapeutic areas and clinical phases.
* Present at industry conferences.
* Engage in peer mentoring and/or line management.
* Develop innovative solutions for study reporting.
* Contribute to B Corp initiatives supporting employees, the environment, and the community.
What to Expect
* A warm, collaborative environment for both personal and professional growth.
* Supportive management with an open-door policy to guide your development.
* Exposure to diverse clients and projects, including collaborations with top pharma companies.
* A unique, forward-thinking CRO that prioritizes staff well-being and innovative project management.
* The opportunity to take ownership of your role and expand your skills.
Beneficial Experience
* Knowledge of the clinical drug development process and relevant disease areas.
* Awareness of industry standards and ICH guidelines.
* Proficiency in SAS or other statistical software (e.g., R), based on your level of experience.
* Strong understanding of CDISC data standards.
* Excellent time-management and self-management skills for competing priorities.
* Ability to work independently and as part of a collaborative team.
If you\'re passionate about delivering high-quality deliverables, enjoy mentoring, and want to make a real impact at a company that values your contribution, this role is for you. We offer flexible working options (home or office), comprehensive training, and a competitive package. Apply now!
As an organisation that has people at the heart of it, Veramed is committed to creating a diverse environment and is proud to be an equal opportunities employer. We foster a working culture where employees have integrity, honesty and respect for one another without regard to, ,, or expression, or. All qualified applicants will receive equal consideration for employment.
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