Senior/Principal Clinical R Programmer

Veramed prides itself on two key areas: providing the highest quality statistics and programming consultancy for its clients, and giving its employees an industry leading working environment with support and training for career growth.

Total Experience : 2 - 6 years

We are seeking a hands on Programmer with attention to detail and strong work ethic to work as part of the statistical and programming team providing programming support as outlined below to a variety of clients in the Veramed portfolio.

This role provides the opportunity to progress towards becoming a Lead Programmer at Veramed.

Key Responsibilities :

- Program and QC datasets and TFLs following specifications and good programming practice.

- Develop dataset specifications that conform to CDISC data standards.

- Attend and contribute to internal and client study team meetings.

- Mentor less experienced members of the team.

Daily Interactions :

- Communicate directly with other study team members and client key contacts.

- Share updates on ongoing work internally and at client meetings.

- Collaborate with the internal Veramed team to deliver high quality work on time and to budget.

- Contribute programming expertise and wider industry knowledge as required.

- Provide support and mentoring for more inexperienced members on the team.

Opportunities For :

- Development into lead programmer or technical role.

- Gaining experience across different therapeutic areas and phases.

- Presenting at conferences.

- Peer mentoring and/or line management.

- Developing innovative solutions to aid study reporting.

- Contributing to initiatives that consider employees, the environment and our local communities as part of our B Corp accreditation.

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.

- Exposure to a wide range of clients and projects, allowing you to diversify your workload and work closely with some of the biggest pharma companies in the industry.

- Work with a truly unique CRO thats doing something different when it comes to managing staff, projects and building relationships in the industry.

- The ability to truly own your role and develop your skills and experience.

Beneficial Experience :

- Understanding of the clinical drug development process and relevant disease areas.

- Awareness of industry and project standards as well as ICH guidelines.

- Proficiency in using R software.

- A good understanding of CDISC data standards.

- Self-management skills with a focus on results for timely and accurate completion of competing deliverables.

- Ability to work independently and as part of a team.