Senior/Principal Statistical Programmer

As a Senior/ Principal Statistical Programmer at Veramed, you will be part of a team that prides itself on providing high-quality statistics and programming consultancy to clients. Your role will involve hands-on programming with attention to detail and a strong work ethic, aiming 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 conforming to CDISC data standards. - Attend and contribute to internal and client study team meetings. - Mentor less experienced team members. - Communicate directly with study team members and client key contacts. - Share updates on ongoing work internally and at client meetings. - Collaborate with the Veramed team to deliver high-quality work on time and to budget. - Provide support and mentoring for less experienced team members. - Opportunities for development into a lead programmer or technical role, gaining experience across different therapeutic areas and phases, presenting at conferences, peer mentoring, line management, and contributing to innovative study reporting solutions. What to Expect: - A warm, friendly working environment conducive to personal and professional growth. - Supportive, open-door management policy aiding in your development. - Exposure to a diverse range of clients and projects. - Work with a unique CRO focusing on managing staff, projects, and building industry relationships differently. - Ownership of your role and opportunities for skill and experience development. Beneficial Experience: - Understanding of the clinical drug development process and relevant disease areas. - Awareness of industry and project standards including ICH guidelines. - Proficiency in SAS or other statistical software (e.g., R) appropriate to the level of seniority. - Good understanding of CDISC data standards. - Self-management skills focusing on timely and accurate completion of deliverables. - Ability to work independently and as part of a team. If you have a passion for delivering high-quality work, enjoy collaborating with team members of all experience levels, and seek a company where you can add value, this role at Veramed could be the right fit for you. Apply now to be part of a diverse environment committed to equal opportunities and fostering a culture of integrity, honesty, and respect for all employees. As a Senior/ Principal Statistical Programmer at Veramed, you will be part of a team that prides itself on providing high-quality statistics and programming consultancy to clients. Your role will involve hands-on programming with attention to detail and a strong work ethic, aiming 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 conforming to CDISC data standards. - Attend and contribute to internal and client study team meetings. - Mentor less experienced team members. - Communicate directly with study team members and client key contacts. - Share updates on ongoing work internally and at client meetings. - Collaborate with the Veramed team to deliver high-quality work on time and to budget. - Provide support and mentoring for less experienced team members. - Opportunities for development into a lead programmer or technical role, gaining experience across different therapeutic areas and phases, presenting at conferences, peer mentoring, line management, and contributing to innovative study reporting solutions. What to Expect: - A warm, friendly working environment conducive to personal and professional growth. - Supportive, open-door management policy aiding in your development. - Exposure to a diverse range of clients and projects. - Work with a unique CRO focusing on managing staff, projects, and building industry relationships differently. - Ownership of your role and opportunities for skill and experience development. Beneficial Experience: - Understanding of the clinical drug development process and relevant disease areas. - Awareness of industry and project standards including ICH guidelines. - Proficiency in SAS or other statistical software (e.g., R) appropriate to the level of seniority. - Good understanding of CDISC data standards. - Self-management skills focusing on timely and accurate completion of deliverables. - Ability to work independently and as part of a team. If you have a passion for delivering high-quality work, enjoy collaborating with team members of all experience levels, and seek a company where you can add value, this role at Veramed could be the right fit for you. Apply now to be part of a diverse environment committed to equal opportunities and fostering a culture of integrity, honesty, and respect for all employees.