Website:
veramed.com
Job details:
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, for experienced PK/PD professionals to work on innovative studies, expand their skills and advance their careers within a supportive, specialist CRO A warm, friendly working environment in which to thrive both personally and professionally. 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.
About the Role
We have multiple exciting opportunities for Lead level Statistical Programmers - who have expertise in R, PK/PD, leading studies. We offer 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 Lead Programmer may also perform a supervisory role (e.g. line management and/or project management).
Responsibilities
- Develop and validate PK analysis datasets and displays (e.g., such as ADPC, ADNCA, ADPP and corresponding displays).
- Generate tables, listings, and figures (TLFs) for PK analysis and reporting.
- Partner with Clinical Pharmacol ogists, Statisticians, and Study Lead Programmers to understand analysis requirements and translate them into effective implementation programmatically.
- Act as subject matter expert (SME) for PK analysis programming.
- Communicates complex PK and analytic al concepts 2 of 2 clearly and concisely, ensuring effective collaboration and alignment within and cross -functional stakeholders.
- Develop and validate PK parameters such as Cmax, Tmax, AUC, Half-life, Clearance, and Volume of Distribution.
- Support population PK (PopPK) and exposure-response analyses.
- Perform QC of PK/PD outputs and ensure regulatory compliance.
- Intermediate to advanced programming skills in R.
- Expertise in CDISC standards, PK workflows of various study designs and implementation.
Work closely with Clinical Pharmacologists, Pharmacometricians, and Biostatisticians.
Qualifications
- BSc, MSc or PhD in numerical discipline (or relevant equivalent industry experience).
- 8 years of hands-on statistical programming experience.
- Mandatory hands- on experience working on PK/PD studies
Required Skills
- R programming.
- CDISC standards (SDTM, ADaM).
- PK software exposure (Phoenix WinNonlin, NONMEM, Monolix is a plus).
- Clinical trials and regulatory submission experience.
About Company:
Veramed is a biometrics-focused CRO, primarily specializing in Statistics and Statistical Programming. Recently, we have also started expanding into Data Management and are in the process of building dedicated data management teams across the UK, US, and India. The company was founded in 2012 by Matthew Jones, a Statistical Programmer, and Emma Jones, a Statistician. Over the past 13 years, Veramed has grown significantly and now has a global workforce of around 750-800+ employees. We have a strong international presence, with three offices in the UK, two offices in Ukraine, and teams located in Spain, Germany, France, and the United States. In India, we launched our operations in March 2024, and within just two years we have grown to 170 employees, including contractors. Currently, we have an office in Bangalore, and our second office in Hyderabad will be launching soon. One of our key strengths is our employee retention, with a strong retention rate of around 92–93% globally. This role offers an excellent opportunity to work alongside experienced professionals, contribute to meaningful clinical research projects, and further develop your technical and programming skills in a collaborative environment
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